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dbVar

Database of genomic structural variation

nsv5617444

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

Submitted genomic10,399,478-10,399,478

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5617444	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	10,399,478	10,399,478
nsv5617444	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	10,539,604	10,539,604

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17107442	insertion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17107442	Submitted genomic		NC_000002.12:g.103 99478_10399479ins8 05	GRCh38 (hg38)		NC_000002.12	Chr2	10,399,478	10,399,478
nssv17107442	Remapped	Perfect	NC_000002.11:g.105 39604_10539605ins8 05	GRCh37.p13	First Pass	NC_000002.11	Chr2	10,539,604	10,539,604

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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