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dbVar

Database of genomic structural variation

nsv5608725

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: 170 SVs from 33 studies. See in: genome view

Submitted genomic88,798,963-88,798,963

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5608725	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	88,798,963	88,798,963
nsv5608725	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	89,264,646	89,264,646

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17067292	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17067292	Submitted genomic		NC_000001.11:g.887 98963_88798964ins3 13	GRCh38 (hg38)		NC_000001.11	Chr1	88,798,963	88,798,963
nssv17067292	Remapped	Perfect	NC_000001.10:g.892 64646_89264647ins3 13	GRCh37.p13	First Pass	NC_000001.10	Chr1	89,264,646	89,264,646

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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