A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5859n100



Internal ID22791946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181015388..181112713hg38UCSC Ensembl
chr5:180442388..180539713hg19UCSC Ensembl
chr5:180374994..180472319hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3897326
hg1997326
hg1897326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022892, nsv1028069, nsv1021707, nsv1029782
Samples
Known GenesBTNL9, MIR8089
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5859n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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