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dbVar

Database of genomic structural variation

nsv5972925

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

Submitted genomic43,447,859-43,447,859

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972925	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	43,447,859	43,447,859
nsv5972925	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	43,843,766	43,843,766

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17404145	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17404145	Submitted genomic		NC_000022.11:g.434 47859_43447860ins2 83	GRCh38 (hg38)		NC_000022.11	Chr22	43,447,859	43,447,859
nssv17404145	Remapped	Perfect	NC_000022.10:g.438 43766_43843767ins2 83	GRCh37.p13	First Pass	NC_000022.10	Chr22	43,843,766	43,843,766

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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