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

dbVar

Database of genomic structural variation

nsv6594810

Organism: Homo sapiens

Study:nstd223 (Sedlazeck et al. 2020)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:75,521

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: 323 SVs from 46 studies. See in: genome view

Submitted genomic117,134,523-117,210,043

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6594810	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	117,134,523	117,210,043
nsv6594810	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	117,005,239	117,080,759

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18226414	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18226414	Submitted genomic		NC_000011.10:g.117 134523_117210043in v	GRCh38 (hg38)		NC_000011.10	Chr11	117,134,523	117,210,043
nssv18226414	Remapped	Perfect	NC_000011.9:g.1170 05239_117080759inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	117,005,239	117,080,759

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)
nssv18226414	0.417	12136	29136

You are here: NCBI