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dbVar

Database of genomic structural variation

nsv4720580

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:nsv4533711 from gnomAD Structural Variants. 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: 113 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):26,178,883-26,178,883

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4720580	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	26,178,883	26,178,883
nsv4720580	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	26,401,752	26,401,752

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16218095	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16218095	Remapped	Perfect	NC_000002.12:g.261 78883_26178884ins?	GRCh38.p12	First Pass	NC_000002.12	Chr2	26,178,883	26,178,883
nssv16218095	Submitted genomic		NC_000002.11:g.264 01752_26401753ins?	GRCh37 (hg19)		NC_000002.11	Chr2	26,401,752	26,401,752

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)
nssv16218095	0.161	3495	21660

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