A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10066n54



Internal ID20143490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128073467..128083046hg38UCSC Ensembl
chr5:127409159..127418738hg19UCSC Ensembl
chr5:127437058..127446637hg18UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg389580
hg199580
hg189580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599678, nsv599695, nsv599683
Samples
Known GenesFLJ33630
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10066n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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