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

dbVar

Database of genomic structural variation

nsv7049599

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:51

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: 133 SVs from 19 studies. See in: genome view

Submitted genomic191,116,490-191,116,540

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7049599	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	191,116,490	191,116,540
nsv7049599	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	191,981,216	191,981,266

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18766578	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
nssv18766578	Submitted genomic		NC_000002.12:g.191 116490_191116540in v	GRCh38 (hg38)		NC_000002.12	Chr2	191,116,490	191,116,540
nssv18766578	Remapped	Perfect	NC_000002.11:g.191 981216_191981266in v	GRCh37.p13	First Pass	NC_000002.11	Chr2	191,981,216	191,981,266

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)
nssv18766578	5.7e-05	16	274710

You are here: NCBI