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dbVar

Database of genomic structural variation

nsv5572986

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

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: 109 SVs from 25 studies. See in: genome view

Submitted genomic71,437,311-71,437,368

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5572986	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	71,437,311	71,437,368
nsv5572986	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	70,733,138	70,733,195

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17158303	deletion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17158303	Submitted genomic		NC_000005.10:g.714 37311_71437368delC	GRCh38 (hg38)		NC_000005.10	Chr5	71,437,311	71,437,368
nssv17158303	Remapped	Perfect	NC_000005.9:g.7073 3138_70733195delC	GRCh37.p13	First Pass	NC_000005.9	Chr5	70,733,138	70,733,195

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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