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dbVar

Database of genomic structural variation

nsv5622885

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 604 SVs from 43 studies. See in: genome view

Submitted genomic2,212,064-2,212,064

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5622885	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	2,212,064	2,212,064
nsv5622885	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	2,143,503	2,143,503

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17063403	insertion	NA24385	Sequencing	Sequence alignment	2,573

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17063403	Submitted genomic		NC_000001.11:g.221 2064_2212065ins459	GRCh38 (hg38)		NC_000001.11	Chr1	2,212,064	2,212,064
nssv17063403	Remapped	Perfect	NC_000001.10:g.214 3503_2143504ins459	GRCh37.p13	First Pass	NC_000001.10	Chr1	2,143,503	2,143,503

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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