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dbVar

Database of genomic structural variation

nsv1155714

Organism: Homo sapiens

Study:nstd97 (Lou et al. 2014)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:148,203

Publication(s):Lou et al. 2014

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: 698 SVs from 60 studies. See in: genome view

Remapped(Score: Good):21,931,691-22,079,893

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv1155714	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	21,931,691	21,931,691	22,079,893	22,079,893
nsv1155714	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	23,304,011	23,309,131	23,449,997	23,452,212

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv4014805	deletion	SNP array	SNP genotyping analysis	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv4014805	Remapped	Good	NC_000021.9:g.(219 31691_21931691)_(2 2079893_22079893)d el	GRCh38.p12	First Pass	NC_000021.9	Chr21	21,931,691	21,931,691	22,079,893	22,079,893
nssv4014805	Submitted genomic		NC_000021.8:g.(233 04011_23309131)_(2 3449997_23452212)d el	GRCh37 (hg19)		NC_000021.8	Chr21	23,304,011	23,309,131	23,449,997	23,452,212

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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