A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5651n100



Internal ID22791738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:46191134..46389159hg38UCSC Ensembl
chr5:46191236..46389261hg19UCSC Ensembl
chr5:46226993..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38198026
hg19198026
hg18198026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016871, nsv1017681, nsv1028468, nsv1020350, nsv1032169
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)dgv5651n100
Frequency
Sample Size11257
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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