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dbVar

Database of genomic structural variation

nsv6308801

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:nsv5560089 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: 176 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):28,879,593-28,879,644

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6308801	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	28,879,593	28,879,644
nsv6308801	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	28,737,110	28,737,161

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17653525	sva insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17653525	Remapped	Perfect	NC_000008.11:g.288 79593_28879644ins?	GRCh38.p12	First Pass	NC_000008.11	Chr8	28,879,593	28,879,644
nssv17653525	Submitted genomic		NC_000008.10:g.287 37110_28737161ins?	GRCh37 (hg19)		NC_000008.10	Chr8	28,737,110	28,737,161

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)
nssv17653525	0.019	124	6404

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