A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5520n100



Internal ID20157136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:375290..438449hg38UCSC Ensembl
chr5:375405..438564hg19UCSC Ensembl
chr5:428405..491564hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3863160
hg1963160
hg1863160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024690, nsv1024390
Samples
Known GenesAHRR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5520n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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