A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1234n54



Internal ID22769129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66512663..66837372hg38UCSC Ensembl
chr10:68272421..68597130hg19UCSC Ensembl
chr10:67942427..68267136hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38324710
hg19324710
hg18324710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551359, nsv551382, nsv551385, nsv551375, nsv551384
SamplesHGDP01380
Known GenesCTNNA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1234n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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