A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7719n100



Internal ID22793806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130574295..130613872hg38UCSC Ensembl
chr9:133449682..133489259hg19UCSC Ensembl
chr9:132439503..132479080hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3839578
hg1939578
hg1839578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035702, nsv1051594, nsv1048187, nsv1040017, nsv1037601, nsv1039569, nsv1049126
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)dgv7719n100
Frequency
Sample Size11257
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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