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dbVar

Database of genomic structural variation

nsv5668779

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: 428 SVs from 37 studies. See in: genome view

Submitted genomic46,165,486-46,165,486

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5668779	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	46,165,486	46,165,486
nsv5668779	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	47,585,400	47,585,400

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17130781	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17130781	Submitted genomic		NC_000021.9:g.4616 5486_46165487ins15 5	GRCh38 (hg38)		NC_000021.9	Chr21	46,165,486	46,165,486
nssv17130781	Remapped	Perfect	NC_000021.8:g.4758 5400_47585401ins15 5	GRCh37.p13	First Pass	NC_000021.8	Chr21	47,585,400	47,585,400

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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