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dbVar

Database of genomic structural variation

nsv5968837

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: 96 SVs from 20 studies. See in: genome view

Submitted genomic38,526,515-38,526,515

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5968837	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	38,526,515	38,526,515
nsv5968837	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	38,922,520	38,922,520

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17405675	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17405675	Submitted genomic		NC_000022.11:g.385 26515_38526516ins3 27	GRCh38 (hg38)		NC_000022.11	Chr22	38,526,515	38,526,515
nssv17405675	Remapped	Perfect	NC_000022.10:g.389 22520_38922521ins3 27	GRCh37.p13	First Pass	NC_000022.10	Chr22	38,922,520	38,922,520

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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