A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5776n100



Internal ID22791863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108305232..108344634hg38UCSC Ensembl
chr5:107640933..107680335hg19UCSC Ensembl
chr5:107668832..107708234hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3839403
hg1939403
hg1839403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033956, nsv1029462
Samples
Known GenesFBXL17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5776n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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