A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7720n100



Internal ID22793807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130574295..130623589hg38UCSC Ensembl
chr9:133449682..133498976hg19UCSC Ensembl
chr9:132439503..132488797hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3849295
hg1949295
hg1849295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044869, nsv1052963, nsv1045323, nsv1040196, nsv1045756
Samples
Known GenesFUBP3, LOC100272217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7720n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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