A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517376



Internal ID293802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90602710..90602861hg38UCSC Ensembl
chr15:91145942..91146093hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703597
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517376
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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