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dbVar

Database of genomic structural variation

nsv180044

Organism: Homo sapiens

Study:nstd6 (Mills et al. 2006)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:9,653

Publication(s):Mills et al. 2006

Links to Other Resources

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: 150 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):15,458,640-15,468,292

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv180044	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	15,458,640	15,468,292
nsv180044	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	15,439,285	15,448,937
nsv180044	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000020.9	Chr20	15,387,285	15,396,937

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv198622	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv198622	Remapped	Perfect	NC_000020.11:g.154 58640_15468292del9 653	GRCh38.p12	First Pass	NC_000020.11	Chr20	15,458,640	15,468,292
nssv198622	Remapped	Perfect	NC_000020.10:g.154 39285_15448937del9 653	GRCh37.p13	First Pass	NC_000020.10	Chr20	15,439,285	15,448,937
nssv198622	Submitted genomic		NC_000020.9:g.1538 7285_15396937del96 53	NCBI35 (hg17)		NC_000020.9	Chr20	15,387,285	15,396,937

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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