A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527392



Internal ID303493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90641514..90643578hg38UCSC Ensembl
chr15:91184746..91186810hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382065
hg192065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703600
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527392
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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