A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12772n54



Internal ID20146196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78030724..78032621hg38UCSC Ensembl
chr9:80645640..80647537hg19UCSC Ensembl
chr9:79835460..79837357hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381898
hg191898
hg181898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614740, nsv614738, nsv614736, nsv614741, nsv614735, nsv614734, nsv614737
Samples
Known GenesGNAQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12772n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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