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dbVar

Database of genomic structural variation

nsv5625003

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: 110 SVs from 24 studies. See in: genome view

Submitted genomic33,168,257-33,168,257

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5625003	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	33,168,257	33,168,257
nsv5625003	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	33,136,034	33,136,034

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17149755	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17149755	Submitted genomic		NC_000006.12:g.331 68257_33168258ins5 9	GRCh38 (hg38)		NC_000006.12	Chr6	33,168,257	33,168,257
nssv17149755	Remapped	Perfect	NC_000006.11:g.331 36034_33136035ins5 9	GRCh37.p13	First Pass	NC_000006.11	Chr6	33,136,034	33,136,034

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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