A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12765n54



Internal ID22780660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76533460..76545843hg38UCSC Ensembl
chr9:79148376..79160759hg19UCSC Ensembl
chr9:78338196..78350579hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812384
hg1912384
hg1812384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614702, nsv614703, nsv614700, nsv614701, nsv614697
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12765n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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