A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9707n54



Internal ID22777602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28786737..28855176hg38UCSC Ensembl
chr5:28786844..28855283hg19UCSC Ensembl
chr5:28822601..28891040hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3868440
hg1968440
hg1868440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597719, nsv597723, nsv597716, nsv597718
SamplesHGDP00926, HGDP00932
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9707n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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