A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9720n54



Internal ID22777615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34656423..34657292hg38UCSC Ensembl
chr5:34656528..34657397hg19UCSC Ensembl
chr5:34692285..34693154hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38870
hg19870
hg18870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597805, nsv597806, nsv597808
Samples
Known GenesRAI14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9720n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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