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dbVar

Database of genomic structural variation

nsv5672488

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: 153 SVs from 25 studies. See in: genome view

Submitted genomic42,878,858-42,878,858

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5672488	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	42,878,858	42,878,858
nsv5672488	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	43,274,864	43,274,864

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17126028	insertion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17126028	Submitted genomic		NC_000022.11:g.428 78858_42878859ins5 4	GRCh38 (hg38)		NC_000022.11	Chr22	42,878,858	42,878,858
nssv17126028	Remapped	Perfect	NC_000022.10:g.432 74864_43274865ins5 4	GRCh37.p13	First Pass	NC_000022.10	Chr22	43,274,864	43,274,864

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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