A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12628n54



Internal ID20146052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28570654..28942610hg38UCSC Ensembl
chr9:28570652..28942608hg19UCSC Ensembl
chr9:28560652..28932608hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38371957
hg19371957
hg18371957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614005, nsv613987
SamplesHGDP01281
Known GenesLINGO2, MIR873, MIR876
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12628n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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