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dbVar

Database of genomic structural variation

nsv5980162

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: 217 SVs from 21 studies. See in: genome view

Submitted genomic45,223,630-45,223,630

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5980162	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	45,223,630	45,223,630
nsv5980162	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	45,619,511	45,619,511

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17390651	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17390651	Submitted genomic		NC_000022.11:g.452 23630_45223631ins7 2	GRCh38 (hg38)		NC_000022.11	Chr22	45,223,630	45,223,630
nssv17390651	Remapped	Perfect	NC_000022.10:g.456 19511_45619512ins7 2	GRCh37.p13	First Pass	NC_000022.10	Chr22	45,619,511	45,619,511

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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