A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9542n54



Internal ID22777437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1822212..1892645hg38UCSC Ensembl
chr5:1822326..1892759hg19UCSC Ensembl
chr5:1875326..1945759hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3870434
hg1970434
hg1870434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596891, nsv596893, nsv596892
Samples
Known GenesIRX4, LOC101929034
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9542n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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