A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044869



Internal ID19134088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130577940..130618610hg38UCSC Ensembl
Innerchr9:133453327..133493997hg19UCSC Ensembl
Innerchr9:132443148..132483818hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3840671
hg1940671
hg1840671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7720n100
Supporting Variantsnssv3695269, nssv3759833, nssv3695268, nssv3759832
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)nsv1044869
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer