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dbVar

Database of genomic structural variation

nsv5671169

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: 453 SVs from 40 studies. See in: genome view

Submitted genomic46,161,033-46,161,033

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671169	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	46,161,033	46,161,033
nsv5671169	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	47,580,947	47,580,947

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17126750	insertion	HG01114	Sequencing	Sequence alignment	977

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17126750	Submitted genomic		NC_000021.9:g.4616 1033_46161034ins95 4	GRCh38 (hg38)		NC_000021.9	Chr21	46,161,033	46,161,033
nssv17126750	Remapped	Perfect	NC_000021.8:g.4758 0947_47580948ins95 4	GRCh37.p13	First Pass	NC_000021.8	Chr21	47,580,947	47,580,947

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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