A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3887n54



Internal ID20137311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99602384..99606662hg38UCSC Ensembl
chr14:100068721..100072999hg19UCSC Ensembl
chr14:99138474..99142752hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384279
hg194279
hg184279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565742, nsv565759
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3887n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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