A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704436



Internal ID128102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80206571..80206695hg38UCSC Ensembl
chr15:80498913..80499037hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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