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dbVar

Database of genomic structural variation

nsv5657376

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 176 SVs from 33 studies. See in: genome view

Submitted genomic90,647,191-90,647,191

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657376	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	90,647,191	90,647,191
nsv5657376	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	91,190,422	91,190,422

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17099080	insertion	SAMN01096687	Sequencing	Sequence alignment	1,334

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17099080	Submitted genomic		NC_000015.10:g.906 47191_90647192ins5 3	GRCh38 (hg38)		NC_000015.10	Chr15	90,647,191	90,647,191
nssv17099080	Remapped	Perfect	NC_000015.9:g.9119 0422_91190423ins53	GRCh37.p13	First Pass	NC_000015.9	Chr15	91,190,422	91,190,422

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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