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dbVar

Database of genomic structural variation

nsv5660350

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: 127 SVs from 31 studies. See in: genome view

Submitted genomic29,558,730-29,558,730

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660350	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	29,558,730	29,558,730
nsv5660350	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	30,132,867	30,132,867

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17084844	insertion	SAMN00016965	Sequencing	Sequence alignment	1,475

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17084844	Submitted genomic		NC_000013.11:g.295 58730_29558731ins1 22	GRCh38 (hg38)		NC_000013.11	Chr13	29,558,730	29,558,730
nssv17084844	Remapped	Perfect	NC_000013.10:g.301 32867_30132868ins1 22	GRCh37.p13	First Pass	NC_000013.10	Chr13	30,132,867	30,132,867

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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