A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12454n54



Internal ID22780349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:515616..527438hg38UCSC Ensembl
chr9:515616..527438hg19UCSC Ensembl
chr9:505616..517438hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3811823
hg1911823
hg1811823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613017, nsv613016
SamplesHGDP01202, HGDP00460, HGDP00458
Known GenesKANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12454n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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