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dbVar

Database of genomic structural variation

nsv4726011

Organism: Homo sapiens

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

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

Description:nsv4556342 from gnomAD Structural Variants. 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: 99 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):52,696,930-52,696,930

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4726011	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	52,696,930	52,696,930
nsv4726011	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	52,730,946	52,730,946

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16230412	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16230412	Remapped	Perfect	NC_000003.12:g.526 96930_52696931ins?	GRCh38.p12	First Pass	NC_000003.12	Chr3	52,696,930	52,696,930
nssv16230412	Submitted genomic		NC_000003.11:g.527 30946_52730947ins?	GRCh37 (hg19)		NC_000003.11	Chr3	52,730,946	52,730,946

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)
nssv16230412	0.586	12704	21694

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