A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696865



Internal ID15086831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91322607..91325417hg38UCSC Ensembl
Innerchr14:91788951..91791761hg19UCSC Ensembl
Innerchr14:90858704..90861514hg18UCSC Ensembl
Innerchr14:90858704..90861514hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382811
hg192811
hg182811
hg172811
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519459
Supporting Variants
Samples
Known GenesCCDC88C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696865
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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