A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496896



Internal ID273961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28172874..28679000hg38UCSC Ensembl
chr15:28418020..28924146hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38506127
hg19506127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699587
Samples
Known GenesGOLGA8F, GOLGA8G, HERC2, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496896
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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