A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039569



Internal ID19128788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130577940..130609326hg38UCSC Ensembl
Innerchr9:133453327..133484713hg19UCSC Ensembl
Innerchr9:132443148..132474534hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3831387
hg1931387
hg1831387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7719n100
Supporting Variantsnssv3695262, nssv3695260, nssv3759831, nssv3695259, nssv3695261, nssv3695266, nssv3695263, nssv3695265, nssv3695264
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)nsv1039569
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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