A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12260n54



Internal ID22780155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110975569..111151572hg38UCSC Ensembl
chr8:111987798..112163801hg19UCSC Ensembl
chr8:112056974..112232977hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38176004
hg19176004
hg18176004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611885, nsv611886
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12260n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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