A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697237



Internal ID120903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91293106..91293506hg38UCSC Ensembl
chr14:91759450..91759850hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494966
Supporting Variants
Samples
Known GenesCCDC88C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697237
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5292


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