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

dbVar

Database of genomic structural variation

nsv499602

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:32,389

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: 234 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):141,866,325-141,898,713

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499602	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	141,866,325	141,898,713
nsv499602	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	142,187,462	142,219,850
nsv499602	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000006.10	Chr6	142,229,155	142,261,543

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585559	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585559	Remapped	Perfect	NC_000006.12:g.141 866325_141898713in v	GRCh38.p12	First Pass	NC_000006.12	Chr6	141,866,325	141,898,713
nssv585559	Remapped	Perfect	NC_000006.11:g.142 187462_142219850in v	GRCh37.p13	First Pass	NC_000006.11	Chr6	142,187,462	142,219,850
nssv585559	Submitted genomic		NC_000006.10:g.142 229155_142261543in v	NCBI36 (hg18)		NC_000006.10	Chr6	142,229,155	142,261,543

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