A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530704



Internal ID306676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64808970..64811581hg38UCSC Ensembl
chr15:65101169..65103780hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382612
hg192612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530704
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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