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dbVar

Database of genomic structural variation

nsv4764406

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: 469 SVs from 52 studies. See in: genome view

Remapped(Score: Perfect):186,958,138-186,958,138

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4764406	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	186,958,138	186,958,138
nsv4764406	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187542.1	Chr4\|NT_18 7542.1	37,780	37,780
nsv4764406	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	187,879,292	187,879,292

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16287195	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16287195	Remapped	Perfect	NT_187542.1:g.3778 0_37781ins86	GRCh38.p12	Second Pass	NT_187542.1	Chr4\|NT_18 7542.1	37,780	37,780
nssv16287195	Remapped	Perfect	NC_000004.12:g.186 958138_186958139in s86	GRCh38.p12	First Pass	NC_000004.12	Chr4	186,958,138	186,958,138
nssv16287195	Submitted genomic		NC_000004.11:g.187 879292_187879293in s86	GRCh37 (hg19)		NC_000004.11	Chr4	187,879,292	187,879,292

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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