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dbVar

Database of genomic structural variation

nsv4641884

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:47,842

Description:esv3872783 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: 392 SVs from 71 studies. See in: genome view

Remapped(Score: Perfect):44,019,364-44,067,205

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4641884	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	44,019,364	44,067,205
nsv4641884	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	44,488,567	44,536,408

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16192897	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16192897	Remapped	Perfect	NC_000014.9:g.4401 9364_44067205del	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,019,364	44,067,205
nssv16192897	Submitted genomic		NC_000014.8:g.4448 8567_44536408del	GRCh37 (hg19)		NC_000014.8	Chr14	44,488,567	44,536,408

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)
nssv16192897	0.015	77	5008

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