A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5636n100



Internal ID20157252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38936517..39017379hg38UCSC Ensembl
chr5:38936619..39017481hg19UCSC Ensembl
chr5:38972376..39053238hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3880863
hg1980863
hg1880863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034905, nsv1016886
Samples
Known GenesRICTOR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5636n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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