A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1201n54



Internal ID22769096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62206628..62300509hg38UCSC Ensembl
chr10:63966387..64060268hg19UCSC Ensembl
chr10:63636393..63730274hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3893882
hg1993882
hg1893882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551180, nsv551182, nsv551181
SamplesHGDP00133
Known GenesRTKN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1201n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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