A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704125



Internal ID127791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89527684..89572709hg38UCSC Ensembl
chr15:90070915..90115940hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3845026
hg1945026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522654
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704125
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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