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

dbVar

Database of genomic structural variation

nsv6979685

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:64,516

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: 427 SVs from 69 studies. See in: genome view

Submitted genomic22,293,372-22,357,887

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6979685	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	22,293,372	22,357,887
nsv6979685	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	22,304,693	22,369,208

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18398429	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
nssv18398429	Submitted genomic		NC_000016.10:g.222 93372_22357887del	GRCh38 (hg38)		NC_000016.10	Chr16	22,293,372	22,357,887
nssv18398429	Remapped	Perfect	NC_000016.9:g.2230 4693_22369208del	GRCh37.p13	First Pass	NC_000016.9	Chr16	22,304,693	22,369,208

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)
nssv18398429	7e-06	2	276078

You are here: NCBI