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

dbVar

Database of genomic structural variation

nsv6826957

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:1,268,120

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: 5299 SVs from 110 studies. See in: genome view

Submitted genomic100,918,010-102,186,129

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6826957	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	100,918,010	102,186,129
nsv6826957	Remapped	Pass	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	100,515,630	101,718,950

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18534371	deletion	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
nssv18534371	Submitted genomic		NC_000007.14:g.100 918010_102186129de l	GRCh38 (hg38)		NC_000007.14	Chr7	100,918,010	102,186,129
nssv18534371	Remapped	Pass	NC_000007.13:g.100 515630_101718950de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	100,515,630	101,718,950

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)
nssv18534371	4e-06	1	276178

You are here: NCBI