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

dbVar

Database of genomic structural variation

nsv499500

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:12,970

Publication(s):Kidd et al. 2010

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: 181 SVs from 47 studies. See in: genome view

Remapped(Score: Good):80,451,138-80,464,107

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499500	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	80,451,138	80,464,107
nsv499500	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	80,844,918	80,857,886
nsv499500	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000012.10	Chr12	79,369,049	79,382,017

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585502	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585502	Remapped	Good	NC_000012.12:g.804 51138_80464107inv	GRCh38.p12	First Pass	NC_000012.12	Chr12	80,451,138	80,464,107
nssv585502	Remapped	Perfect	NC_000012.11:g.808 44918_80857886inv	GRCh37.p13	First Pass	NC_000012.11	Chr12	80,844,918	80,857,886
nssv585502	Submitted genomic		NC_000012.10:g.793 69049_79382017inv	NCBI36 (hg18)		NC_000012.10	Chr12	79,369,049	79,382,017

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

You are here: NCBI