A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5753n100



Internal ID22791840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:104168143..104201752hg38UCSC Ensembl
chr5:103503844..103537453hg19UCSC Ensembl
chr5:103531743..103565352hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3833610
hg1933610
hg1833610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031549, nsv1030270, nsv1019806, nsv1027894, nsv1026088, nsv1033955, nsv1025874, nsv1029475, nsv1027980
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)dgv5753n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss84
Observed Complex0
Frequencyn/a


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