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

dbVar

Database of genomic structural variation

nsv6112170

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,017,584

Publication(s):Wu et al. 2021

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: 6617 SVs from 117 studies. See in: genome view

Submitted genomic175,902,456-177,920,039

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112170	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	175,902,456	177,920,039
nsv6112170	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	175,329,459	177,347,040

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17565023	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17565023	Submitted genomic		NC_000005.10:g.175 902456_177920039in v	GRCh38 (hg38)		NC_000005.10	Chr5	175,902,456	177,920,039
nssv17565023	Remapped	Perfect	NC_000005.9:g.1753 29459_177347040inv	GRCh37.p13	First Pass	NC_000005.9	Chr5	175,329,459	177,347,040

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI