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

dbVar

Database of genomic structural variation

nsv6813051

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:6,900

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: 111 SVs from 25 studies. See in: genome view

Submitted genomic151,521,901-151,528,800

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6813051	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	151,521,901	151,528,800
nsv6813051	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	151,843,036	151,849,935

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18522816	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
nssv18522816	Submitted genomic		NC_000006.12:g.151 521901_151528800de l	GRCh38 (hg38)		NC_000006.12	Chr6	151,521,901	151,528,800
nssv18522816	Remapped	Perfect	NC_000006.11:g.151 843036_151849935de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	151,843,036	151,849,935

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)
nssv18522816	4e-06	1	276098

You are here: NCBI