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

dbVar

Database of genomic structural variation

nsv5562484

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:74

Publication(s):Byrska-Bishop et al. 2022

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: 109 SVs from 30 studies. See in: genome view

Submitted genomic93,906,947-93,907,020

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5562484	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	93,906,947	93,907,020
nsv5562484	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	93,536,259	93,536,332

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17000382	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17000382	Submitted genomic		NC_000007.14:g.939 06947_93907020inv	GRCh38 (hg38)		NC_000007.14	Chr7	93,906,947	93,907,020
nssv17000382	Remapped	Perfect	NC_000007.13:g.935 36259_93536332inv	GRCh37.p13	First Pass	NC_000007.13	Chr7	93,536,259	93,536,332

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)
nssv17000382	0.052	336	6404

You are here: NCBI