A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12831n54



Internal ID19005007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104840397..104914659hg38UCSC Ensembl
chr9:107602678..107676940hg19UCSC Ensembl
chr9:106642499..106716761hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3874263
hg1974263
hg1874263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615082, nsv615085
Samples1780862197_A
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12831n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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