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

dbVar

Database of genomic structural variation

nsv2816945

Organism: Homo sapiens

Study:nstd137 (Huddleston et al. 2016)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,076

Publication(s):Huddleston et al. 2016

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: 140 SVs from 44 studies. See in: genome view

Submitted genomic40,839,789-40,840,864

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv2816945	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	40,839,789	40,840,864
nsv2816945	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	40,879,388	40,880,463

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv13703390	inversion	SAMN02744161	Sequencing	Local sequence assembly	47

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv13703390	Submitted genomic		NC_000007.14:g.408 39789_40840864inv	GRCh38 (hg38)		NC_000007.14	Chr7	40,839,789	40,840,864
nssv13703390	Remapped	Perfect	NC_000007.13:g.408 79388_40880463inv	GRCh37.p13	First Pass	NC_000007.13	Chr7	40,879,388	40,880,463

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