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dbVar

Database of genomic structural variation

nsv6293918

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:52

Description:nsv5409494 from Byrska-Bishop et. al 2021. 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: 92 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):46,296,475-46,296,526

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6293918	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	46,296,475	46,296,526
nsv6293918	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	46,318,026	46,318,077

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17655960	alu insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17655960	Remapped	Perfect	NC_000011.10:g.462 96475_46296526ins?	GRCh38.p12	First Pass	NC_000011.10	Chr11	46,296,475	46,296,526
nssv17655960	Submitted genomic		NC_000011.9:g.4631 8026_46318077ins?	GRCh37 (hg19)		NC_000011.9	Chr11	46,318,026	46,318,077

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)
nssv17655960	0.431	2730	6340

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