A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704796



Internal ID128462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100774090..100774570hg38UCSC Ensembl
chr15:101314295..101314775hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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