A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046733



Internal ID18789264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91928340..92376282hg38UCSC Ensembl
Innerchr9:94690622..95138564hg19UCSC Ensembl
Innerchr9:93730443..94178385hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38447943
hg19447943
hg18447943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697551
Samples
Known GenesCENPP, IARS, LINC00475, LOC100128076, MIR3651, NOL8, ROR2, SNORA84, SPTLC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046733
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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