A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5781n100



Internal ID20157397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111079513..111107582hg38UCSC Ensembl
chr5:110415211..110443281hg19UCSC Ensembl
chr5:110443110..110471180hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3828070
hg1928071
hg1828071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026217, nsv1029630, nsv1017520, nsv1020835, nsv1020352, nsv1032893, nsv1024198, nsv1032342, nsv1019553, nsv1030574, nsv1023278
Samples
Known GenesWDR36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5781n100
Frequency
Sample Size29084
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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