A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5806n100



Internal ID22791893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121600538..121706542hg38UCSC Ensembl
chr5:120936233..121042237hg19UCSC Ensembl
chr5:120964132..121070136hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38106005
hg19106005
hg18106005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015593, nsv1020519, nsv1018017, nsv1034402, nsv1027506
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)dgv5806n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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