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dbVar

Database of genomic structural variation

nsv5980362

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

Links to Other Resources

Overlapping Genes

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: 138 SVs from 19 studies. See in: genome view

Submitted genomic88,522,512-88,522,512

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5980362	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	88,522,512	88,522,512
nsv5980362	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	89,065,743	89,065,743

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17375697	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17375697	Submitted genomic		NC_000015.10:g.885 22512_88522513ins1 67	GRCh38 (hg38)		NC_000015.10	Chr15	88,522,512	88,522,512
nssv17375697	Remapped	Perfect	NC_000015.9:g.8906 5743_89065744ins16 7	GRCh37.p13	First Pass	NC_000015.9	Chr15	89,065,743	89,065,743

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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