A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12880n54



Internal ID22780775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127790636..127857358hg38UCSC Ensembl
chr9:130552915..130619637hg19UCSC Ensembl
chr9:129592736..129659458hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3866723
hg1966723
hg1866723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615375, nsv615376
SamplesHGDP00688
Known GenesCDK9, ENG, FPGS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12880n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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