A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5956n100



Internal ID20157572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35508785..35611598hg38UCSC Ensembl
chr6:35476562..35579375hg19UCSC Ensembl
chr6:35584540..35687353hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38102814
hg19102814
hg18102814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031987, nsv1032973, nsv1022435, nsv1034786
Samples
Known GenesFKBP5, TULP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5956n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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