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dbVar

Database of genomic structural variation

nsv499805

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:276,359

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: 873 SVs from 74 studies. See in: genome view

Remapped(Score: Perfect):170,425,280-170,701,638

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499805	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	170,425,280	170,701,638
nsv499805	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	171,346,431	171,622,789
nsv499805	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000004.10	Chr4	171,583,006	171,859,364

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585550	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585550	Remapped	Perfect	NC_000004.12:g.170 425280_170701638in v	GRCh38.p12	First Pass	NC_000004.12	Chr4	170,425,280	170,701,638
nssv585550	Remapped	Perfect	NC_000004.11:g.171 346431_171622789in v	GRCh37.p13	First Pass	NC_000004.11	Chr4	171,346,431	171,622,789
nssv585550	Submitted genomic		NC_000004.10:g.171 583006_171859364in v	NCBI36 (hg18)		NC_000004.10	Chr4	171,583,006	171,859,364

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

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