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dbVar

Database of genomic structural variation

nsv6130653

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:16

Description:nsv5539969 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: 105 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):61,620,206-61,620,221

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130653	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	61,620,206	61,620,221
nsv6130653	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	60,195,262	60,195,277

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17959856	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17959856	Remapped	Perfect	NC_000020.11:g.616 20206_61620221ins?	GRCh38.p12	First Pass	NC_000020.11	Chr20	61,620,206	61,620,221
nssv17959856	Submitted genomic		NC_000020.10:g.601 95262_60195277ins?	GRCh37 (hg19)		NC_000020.10	Chr20	60,195,262	60,195,277

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)
nssv17959856	0.48	3074	6404

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