A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040196



Internal ID19129415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130577940..130623589hg38UCSC Ensembl
Innerchr9:133453327..133498976hg19UCSC Ensembl
Innerchr9:132443148..132488797hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3845650
hg1945650
hg1845650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7720n100
Supporting Variantsnssv3759836, nssv3759837
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)nsv1040196
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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