A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5777n100



Internal ID22791864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109932371..110028680hg38UCSC Ensembl
chr5:109268072..109364381hg19UCSC Ensembl
chr5:109295971..109392280hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3896310
hg1996310
hg1896310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030510, nsv1028449, nsv1016254, nsv1033605
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)dgv5777n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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