A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12660n54



Internal ID22780555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34957616..34958572hg38UCSC Ensembl
chr9:34957613..34958569hg19UCSC Ensembl
chr9:34947613..34948569hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38957
hg19957
hg18957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614161, nsv614160, nsv614159, nsv614158
Samples
Known GenesKIAA1045
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12660n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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