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

dbVar

Database of genomic structural variation

nsv7076939

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:7,160,922

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: 20715 SVs from 139 studies. See in: genome view

Submitted genomic15,569,413-22,730,334

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7076939	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	15,569,413	22,730,334
nsv7076939	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	15,663,270	22,741,655

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18757491	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
nssv18757491	Submitted genomic		NC_000016.10:g.155 69413_22730334inv	GRCh38 (hg38)		NC_000016.10	Chr16	15,569,413	22,730,334
nssv18757491	Remapped	Good	NC_000016.9:g.1566 3270_22741655inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	15,663,270	22,741,655

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)
nssv18757491	4e-06	1	276268

You are here: NCBI