A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3893n54



Internal ID20137317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99603341..99604392hg38UCSC Ensembl
chr14:100069678..100070729hg19UCSC Ensembl
chr14:99139431..99140482hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381052
hg191052
hg181052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565756, nsv565757, nsv565761
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3893n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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