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dbVar

Database of genomic structural variation

nsv5643641

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: 215 SVs from 39 studies. See in: genome view

Submitted genomic31,498,593-31,498,593

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5643641	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	31,498,593	31,498,593
nsv5643641	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	31,466,370	31,466,370

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17143928	insertion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17143928	Submitted genomic		NC_000006.12:g.314 98593_31498594ins1 79	GRCh38 (hg38)		NC_000006.12	Chr6	31,498,593	31,498,593
nssv17143928	Remapped	Perfect	NC_000006.11:g.314 66370_31466371ins1 79	GRCh37.p13	First Pass	NC_000006.11	Chr6	31,466,370	31,466,370

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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