A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532576



Internal ID308495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72397355..72441960hg38UCSC Ensembl
chr15:72689696..72734301hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3844606
hg1944606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702434
Samples
Known GenesTMEM202
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532576
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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