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dbVar

Database of genomic structural variation

nsv6308893

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:52

Description:nsv5559505 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: 146 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):89,785,648-89,785,699

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6308893	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	89,785,648	89,785,699
nsv6308893	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	90,706,799	90,706,850

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17664599	line1 insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17664599	Remapped	Perfect	NC_000004.12:g.897 85648_89785699ins?	GRCh38.p12	First Pass	NC_000004.12	Chr4	89,785,648	89,785,699
nssv17664599	Submitted genomic		NC_000004.11:g.907 06799_90706850ins?	GRCh37 (hg19)		NC_000004.11	Chr4	90,706,799	90,706,850

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)
nssv17664599	0.116	683	5870

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