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dbVar

Database of genomic structural variation

nsv5649755

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

Submitted genomic40,808,646-40,808,646

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5649755	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	40,808,646	40,808,646
nsv5649755	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	41,382,782	41,382,782

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17084463	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
nssv17084463	Submitted genomic		NC_000013.11:g.408 08646_40808647ins1 74	GRCh38 (hg38)		NC_000013.11	Chr13	40,808,646	40,808,646
nssv17084463	Remapped	Perfect	NC_000013.10:g.413 82782_41382783ins1 74	GRCh37.p13	First Pass	NC_000013.10	Chr13	41,382,782	41,382,782

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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