A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5564n100



Internal ID22791651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8699653..8752606hg38UCSC Ensembl
chr5:8699765..8752718hg19UCSC Ensembl
chr5:8752765..8805718hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3852954
hg1952954
hg1852954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032657, nsv1019577, nsv1026284, nsv1028939, nsv1029834, nsv1022347, nsv1027194, nsv1021415, nsv1027474, nsv1019724, nsv1027787, nsv1022569, nsv1027237, nsv1016301, nsv1018839, nsv1016033, nsv1031325, nsv1021627, nsv1030265, nsv1032517, nsv1026017, nsv1028674, nsv1020362, nsv1016440
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)dgv5564n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss466
Observed Complex0
Frequencyn/a


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