A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10302n54



Internal ID20143726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13944836..14014562hg38UCSC Ensembl
chr6:13945067..14014793hg19UCSC Ensembl
chr6:14053046..14122772hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3869727
hg1969727
hg1869727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600996, nsv600995
Samples
Known GenesRNF182
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10302n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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