A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702472



Internal ID126138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75600089..75609413hg38UCSC Ensembl
chr15:75892430..75901754hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg389325
hg199325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522469
Supporting Variants
Samples
Known GenesSNUPN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702472
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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