A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703597



Internal ID127263
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 StatusS
Merged Variantsnsv5517376
Supporting Variants
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703597
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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