A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12829n54



Internal ID19005005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104833924..104834976hg38UCSC Ensembl
chr9:107596205..107597257hg19UCSC Ensembl
chr9:106636026..106637078hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381053
hg191053
hg181053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615079, nsv615078, nsv615077, nsv615073, nsv615072
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12829n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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