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dbVar

Database of genomic structural variation

nsv6130227

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:37

Description:nsv5546662 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: 129 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):61,877,453-61,877,489

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130227	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	61,877,453	61,877,489
nsv6130227	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	62,169,652	62,169,688

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17964236	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17964236	Remapped	Perfect	NC_000015.10:g.618 77453_61877489ins?	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,877,453	61,877,489
nssv17964236	Submitted genomic		NC_000015.9:g.6216 9652_62169688ins?	GRCh37 (hg19)		NC_000015.9	Chr15	62,169,652	62,169,688

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)
nssv17964236	0.197	1257	6374

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