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dbVar

Database of genomic structural variation

nsv4716663

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:mobile element insertion
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Description:nsv4487059 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: 95 SVs from 19 studies. See in: genome view

Remapped(Score: Perfect):97,362,666-97,362,666

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4716663	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	97,362,666	97,362,666
nsv4716663	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	100,124,948	100,124,948

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16228834	alu insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16228834	Remapped	Perfect	NC_000009.12:g.973 62666_97362667ins?	GRCh38.p12	First Pass	NC_000009.12	Chr9	97,362,666	97,362,666
nssv16228834	Submitted genomic		NC_000009.11:g.100 124948_100124949in s?	GRCh37 (hg19)		NC_000009.11	Chr9	100,124,948	100,124,948

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)
nssv16228834	0.013	274	21666

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