A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7132n100



Internal ID19017500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21905882..22038705hg38UCSC Ensembl
chr8:21763393..21896216hg19UCSC Ensembl
chr8:21819339..21952162hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38132824
hg19132824
hg18132824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034576, nsv1032164
Samples
Known GenesDOK2, NPM2, XPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7132n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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