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dbVar

Database of genomic structural variation

nsv5565873

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:124

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: 477 SVs from 63 studies. See in: genome view

Submitted genomic6,998,550-6,998,673

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5565873	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	6,998,550	6,998,673
nsv5565873	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	6,856,072	6,856,195

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17156967	deletion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17156967	Submitted genomic		NC_000008.11:g.699 8550_6998673delA	GRCh38 (hg38)		NC_000008.11	Chr8	6,998,550	6,998,673
nssv17156967	Remapped	Perfect	NC_000008.10:g.685 6072_6856195delA	GRCh37.p13	First Pass	NC_000008.10	Chr8	6,856,072	6,856,195

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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