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dbVar

Database of genomic structural variation

nsv5581743

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:116

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: 164 SVs from 43 studies. See in: genome view

Submitted genomic78,061,615-78,061,730

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5581743	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	78,061,615	78,061,730
nsv5581743	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	78,527,299	78,527,414

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17066447	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17066447	Submitted genomic		NC_000001.11:g.780 61615_78061730delT	GRCh38 (hg38)		NC_000001.11	Chr1	78,061,615	78,061,730
nssv17066447	Remapped	Perfect	NC_000001.10:g.785 27299_78527414delT	GRCh37.p13	First Pass	NC_000001.10	Chr1	78,527,299	78,527,414

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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