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dbVar

Database of genomic structural variation

nsv4751317

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Quan et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 236 SVs from 33 studies. See in: genome view

Remapped(Score: Perfect):154,590,563-154,590,563

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4751317	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	154,590,563	154,590,563
nsv4751317	Remapped	Perfect	GRCh38.p12	PATCHES	Second Pass	NW_012132919.1	Chr7\|NW_01 2132919.1	167,558	167,558
nsv4751317	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	154,382,273	154,382,273

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16283887	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16283887	Remapped	Perfect	NW_012132919.1:g.1 67558_167559ins318	GRCh38.p12	Second Pass	NW_012132919.1	Chr7\|NW_01 2132919.1	167,558	167,558
nssv16283887	Remapped	Perfect	NC_000007.14:g.154 590563_154590564in s318	GRCh38.p12	First Pass	NC_000007.14	Chr7	154,590,563	154,590,563
nssv16283887	Submitted genomic		NC_000007.13:g.154 382273_154382274in s318	GRCh37 (hg19)		NC_000007.13	Chr7	154,382,273	154,382,273

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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