A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5797n100



Internal ID22791884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120687722..120797095hg38UCSC Ensembl
chr5:120023417..120132790hg19UCSC Ensembl
chr5:120051316..120160689hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38109374
hg19109374
hg18109374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022693, nsv1016516
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)dgv5797n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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