A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5862n100



Internal ID20157478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181136493..181229128hg38UCSC Ensembl
chr5:180563493..180656128hg19UCSC Ensembl
chr5:180496099..180588734hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3892636
hg1992636
hg1892636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031000, nsv1033380
Samples
Known GenesLOC102577426, MIR4638, OR2V2, TRIM41, TRIM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5862n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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