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dbVar

Database of genomic structural variation

nsv6130535

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:36

Description:nsv5542111 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: 94 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):40,024,244-40,024,279

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130535	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	40,024,244	40,024,279
nsv6130535	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	40,316,445	40,316,480

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17964110	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17964110	Remapped	Perfect	NC_000015.10:g.400 24244_40024279ins?	GRCh38.p12	First Pass	NC_000015.10	Chr15	40,024,244	40,024,279
nssv17964110	Submitted genomic		NC_000015.9:g.4031 6445_40316480ins?	GRCh37 (hg19)		NC_000015.9	Chr15	40,316,445	40,316,480

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)
nssv17964110	0.016	104	6404

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