A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5861n100



Internal ID20157477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181099500..181159791hg38UCSC Ensembl
chr5:180526500..180586791hg19UCSC Ensembl
chr5:180459106..180519397hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3860292
hg1960292
hg1860292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032620, nsv1020299
Samples
Known GenesOR2V1, OR2V2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5861n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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