A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730106



Internal ID153772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5030779..5031938hg38UCSC Ensembl
chr3:5072464..5073623hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg381160
hg191160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730106
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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