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dbVar

Database of genomic structural variation

nsv5658435

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 29 studies. See in: genome view

Submitted genomic88,856,267-88,856,267

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5658435	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	88,856,267	88,856,267
nsv5658435	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	89,399,498	89,399,498

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17082770	insertion	HG01114	Sequencing	Sequence alignment	977

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17082770	Submitted genomic		NC_000015.10:g.888 56267_88856268ins5 9	GRCh38 (hg38)		NC_000015.10	Chr15	88,856,267	88,856,267
nssv17082770	Remapped	Perfect	NC_000015.9:g.8939 9498_89399499ins59	GRCh37.p13	First Pass	NC_000015.9	Chr15	89,399,498	89,399,498

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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