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

dbVar

Database of genomic structural variation

nsv7060613

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,180,579

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: 3668 SVs from 122 studies. See in: genome view

Submitted genomic21,590,269-22,770,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7060613	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	21,590,269	22,770,847
nsv7060613	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	21,601,590	22,782,168

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18756424	inversion	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
nssv18756424	Submitted genomic		NC_000016.10:g.215 90269_22770847inv	GRCh38 (hg38)		NC_000016.10	Chr16	21,590,269	22,770,847
nssv18756424	Remapped	Perfect	NC_000016.9:g.2160 1590_22782168inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	21,601,590	22,782,168

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)
nssv18756424	0.004	1148	274546

You are here: NCBI