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dbVar

Database of genomic structural variation

nsv4655150

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:mobile element deletion
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:349

Description:esv3862439 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: 282 SVs from 55 studies. See in: genome view

Remapped(Score: Perfect):131,060,209-131,060,557

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4655150	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	131,060,209	131,060,557
nsv4655150	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	132,858,472	132,858,820

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16186842	alu deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16186842	Remapped	Perfect	NC_000010.11:g.131 060209_131060557de l	GRCh38.p12	First Pass	NC_000010.11	Chr10	131,060,209	131,060,557
nssv16186842	Submitted genomic		NC_000010.10:g.132 858472_132858820de l	GRCh37 (hg19)		NC_000010.10	Chr10	132,858,472	132,858,820

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)
nssv16186842	0.529	2651	5008

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