A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12853n54



Internal ID20146277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113052193..113104996hg38UCSC Ensembl
chr9:115814473..115867276hg19UCSC Ensembl
chr9:114854294..114907097hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3852804
hg1952804
hg1852804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615205, nsv615206
SamplesHGDP00199, HGDP00692
Known GenesFAM225B, ZFP37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12853n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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