A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12235n54



Internal ID20145659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91110980..91171430hg38UCSC Ensembl
chr8:92123208..92183658hg19UCSC Ensembl
chr8:92192384..92252834hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3860451
hg1960451
hg1860451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611722, nsv611723
SamplesHGDP01057
Known GenesLRRC69
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12235n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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