Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv7015411

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:43,911

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: 240 SVs from 57 studies. See in: genome view

Submitted genomic45,755,392-45,799,302

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7015411	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	45,755,392	45,799,302
nsv7015411	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	46,258,650	46,302,560

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18638610	duplication	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18638610	Submitted genomic		NC_000019.10:g.457 55392_45799302dup	GRCh38 (hg38)		NC_000019.10	Chr19	45,755,392	45,799,302
nssv18638610	Remapped	Perfect	NC_000019.9:g.4625 8650_46302560dup	GRCh37.p13	First Pass	NC_000019.9	Chr19	46,258,650	46,302,560

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18638610	4e-06	1	275626

You are here: NCBI