A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12832n54



Internal ID19005008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104856400..104893567hg38UCSC Ensembl
chr9:107618681..107655848hg19UCSC Ensembl
chr9:106658502..106695669hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3837168
hg1937168
hg1837168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615087, nsv615088
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12832n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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