A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5516n100



Internal ID20157132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17630..81382hg38UCSC Ensembl
chr5:17630..81497hg19UCSC Ensembl
chr5:70630..134497hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3863753
hg1963868
hg1863868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026497, nsv1026902
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5516n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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