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dbVar

Database of genomic structural variation

nsv4757586

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: 292 SVs from 45 studies. See in: genome view

Remapped(Score: Perfect):21,207,623-21,207,623

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4757586	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	21,207,623	21,207,623
nsv4757586	Remapped	Perfect	GRCh38.p12	PATCHES	Second Pass	NW_009646199.1	Chr5\|NW_00 9646199.1	115,748	115,748
nsv4757586	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	21,207,732	21,207,732

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16288850	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16288850	Remapped	Perfect	NW_009646199.1:g.1 15748_115749ins593 6	GRCh38.p12	Second Pass	NW_009646199.1	Chr5\|NW_00 9646199.1	115,748	115,748
nssv16288850	Remapped	Perfect	NC_000005.10:g.212 07623_21207624ins5 936	GRCh38.p12	First Pass	NC_000005.10	Chr5	21,207,623	21,207,623
nssv16288850	Submitted genomic		NC_000005.9:g.2120 7732_21207733ins59 36	GRCh37 (hg19)		NC_000005.9	Chr5	21,207,732	21,207,732

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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