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dbVar

Database of genomic structural variation

nsv4641838

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:353

Description:esv3853331 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: 178 SVs from 49 studies. See in: genome view

Remapped(Score: Perfect):31,713,726-31,714,078

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4641838	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	31,713,726	31,714,078
nsv4641838	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	31,571,242	31,571,594

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16192061	alu deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16192061	Remapped	Perfect	NC_000008.11:g.317 13726_31714078del	GRCh38.p12	First Pass	NC_000008.11	Chr8	31,713,726	31,714,078
nssv16192061	Submitted genomic		NC_000008.10:g.315 71242_31571594del	GRCh37 (hg19)		NC_000008.10	Chr8	31,571,242	31,571,594

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)
nssv16192061	0.716	3588	5008

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