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dbVar

Database of genomic structural variation

nsv4665613

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:10,194

Description:esv3874921 from 1000 Genomes Consortium Phase 3 Integrated SV. For a full list of variants now included in nstd186, refer to the mapping file provided here.

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: 458 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):43,598,985-43,609,178

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4665613	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	43,598,985	43,609,178
nsv4665613	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	43,891,183	43,901,376

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16206137	copy number variation	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16206137	Remapped	Perfect	GRCh38.p12	First Pass	NC_000015.10	Chr15	43,598,985	43,609,178
nssv16206137	Submitted genomic		GRCh37 (hg19)		NC_000015.9	Chr15	43,891,183	43,901,376

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16206137	0.022	109	5008

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