A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3892n54



Internal ID20137316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99603237..99616411hg38UCSC Ensembl
chr14:100069574..100082748hg19UCSC Ensembl
chr14:99139327..99152501hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3813175
hg1913175
hg1813175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565754, nsv565760
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3892n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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