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dbVar

Database of genomic structural variation

nsv5972746

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 381 SVs from 34 studies. See in: genome view

Submitted genomic46,298,434-46,298,434

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972746	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	46,298,434	46,298,434
nsv5972746	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	47,718,348	47,718,348

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17394539	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17394539	Submitted genomic		NC_000021.9:g.4629 8434_46298435ins96	GRCh38 (hg38)		NC_000021.9	Chr21	46,298,434	46,298,434
nssv17394539	Remapped	Perfect	NC_000021.8:g.4771 8348_47718349ins96	GRCh37.p13	First Pass	NC_000021.8	Chr21	47,718,348	47,718,348

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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