A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12792n54



Internal ID22780687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91633240..91641031hg38UCSC Ensembl
chr9:94395522..94403313hg19UCSC Ensembl
chr9:93435343..93443134hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387792
hg197792
hg187792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614858, nsv614862, nsv614861, nsv614859, nsv614864
Samples
Known GenesMIR3910-1, MIR3910-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12792n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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