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dbVar

Database of genomic structural variation

nsv5568336

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:58,256

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: 265 SVs from 47 studies. See in: genome view

Submitted genomic76,918,969-76,977,224

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5568336	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	76,918,969	76,977,224
nsv5568336	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	77,384,654	77,442,909

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17066407	deletion	SAMN00000419	Sequencing	Sequence alignment	1,071

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17066407	Submitted genomic		NC_000001.11:g.769 18969_76977224delT	GRCh38 (hg38)		NC_000001.11	Chr1	76,918,969	76,977,224
nssv17066407	Remapped	Perfect	NC_000001.10:g.773 84654_77442909delT	GRCh37.p13	First Pass	NC_000001.10	Chr1	77,384,654	77,442,909

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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