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dbVar

Database of genomic structural variation

nsv499733

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:10,368

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: 113 SVs from 32 studies. See in: genome view

Remapped(Score: Good):50,887,229-50,897,596

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499733	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	50,887,229	50,897,596
nsv499733	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	50,925,339	50,935,706
nsv499733	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000003.10	Chr3	50,899,679	50,910,048

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585539	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585539	Remapped	Good	NC_000003.12:g.508 87229_50897596inv	GRCh38.p12	First Pass	NC_000003.12	Chr3	50,887,229	50,897,596
nssv585539	Remapped	Good	NC_000003.11:g.509 25339_50935706inv	GRCh37.p13	First Pass	NC_000003.11	Chr3	50,925,339	50,935,706
nssv585539	Submitted genomic		NC_000003.10:g.508 99679_50910048inv	NCBI36 (hg18)		NC_000003.10	Chr3	50,899,679	50,910,048

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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