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dbVar

Database of genomic structural variation

nsv6131281

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:nsv5552946 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: 93 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):31,226,475-31,226,475

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131281	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	31,226,475	31,226,475
nsv6131281	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	31,622,461	31,622,461

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17960359	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17960359	Remapped	Perfect	NC_000022.11:g.312 26475_31226476ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	31,226,475	31,226,475
nssv17960359	Submitted genomic		NC_000022.10:g.316 22461_31622462ins?	GRCh37 (hg19)		NC_000022.10	Chr22	31,622,461	31,622,461

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)
nssv17960359	0.852	5346	6272

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