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

dbVar

Database of genomic structural variation

nsv499606

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:22,945

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: 630 SVs from 83 studies. See in: genome view

Remapped(Score: Perfect):7,811,118-7,834,062

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499606	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	7,811,118	7,834,062
nsv499606	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	7,963,714	7,986,658
nsv499606	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000012.10	Chr12	7,854,981	7,877,925

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585499	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585499	Remapped	Perfect	NC_000012.12:g.781 1118_7834062inv	GRCh38.p12	First Pass	NC_000012.12	Chr12	7,811,118	7,834,062
nssv585499	Remapped	Perfect	NC_000012.11:g.796 3714_7986658inv	GRCh37.p13	First Pass	NC_000012.11	Chr12	7,963,714	7,986,658
nssv585499	Submitted genomic		NC_000012.10:g.785 4981_7877925inv	NCBI36 (hg18)		NC_000012.10	Chr12	7,854,981	7,877,925

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