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dbVar

Database of genomic structural variation

nsv6131012

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:8

Description:nsv5545880 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: 214 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):107,676,629-107,676,636

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131012	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	107,676,629	107,676,636
nsv6131012	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	108,328,977	108,328,984

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17963236	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17963236	Remapped	Perfect	NC_000013.11:g.107 676629_107676636in s?	GRCh38.p12	First Pass	NC_000013.11	Chr13	107,676,629	107,676,636
nssv17963236	Submitted genomic		NC_000013.10:g.108 328977_108328984in s?	GRCh37 (hg19)		NC_000013.10	Chr13	108,328,977	108,328,984

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)
nssv17963236	0.013	81	6392

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