A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524562



Internal ID300764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77136499..77138695hg38UCSC Ensembl
chr15:77428841..77431037hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382197
hg192197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702109
Samples
Known GenesPEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524562
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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