A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7131n100



Internal ID20158747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21905882..21974708hg38UCSC Ensembl
chr8:21763393..21832219hg19UCSC Ensembl
chr8:21819339..21888165hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3868827
hg1968827
hg1868827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034809, nsv1018071, nsv1032704, nsv1017189, nsv1028945, nsv1033234, nsv1034778, nsv1025759, nsv1034330
Samples
Known GenesDOK2, XPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7131n100
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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