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dbVar

Database of genomic structural variation

nsv6127920

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:nsv5536922 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 21 studies. See in: genome view

Remapped(Score: Perfect):178,327,083-178,327,083

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6127920	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	178,327,083	178,327,083
nsv6127920	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	179,191,810	179,191,810

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17660503	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17660503	Remapped	Perfect	NC_000002.12:g.178 327083_178327084in s?	GRCh38.p12	First Pass	NC_000002.12	Chr2	178,327,083	178,327,083
nssv17660503	Submitted genomic		NC_000002.11:g.179 191810_179191811in s?	GRCh37 (hg19)		NC_000002.11	Chr2	179,191,810	179,191,810

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)
nssv17660503	0.012	74	6382

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