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dbVar

Database of genomic structural variation

nsv5973573

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: 428 SVs from 36 studies. See in: genome view

Submitted genomic46,165,546-46,165,546

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5973573	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	46,165,546	46,165,546
nsv5973573	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	47,585,460	47,585,460

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17409357	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17409357	Submitted genomic		NC_000021.9:g.4616 5546_46165547ins19 7	GRCh38 (hg38)		NC_000021.9	Chr21	46,165,546	46,165,546
nssv17409357	Remapped	Perfect	NC_000021.8:g.4758 5460_47585461ins19 7	GRCh37.p13	First Pass	NC_000021.8	Chr21	47,585,460	47,585,460

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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