A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697551



Internal ID18649146
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 StatusS
Merged Variantsnsv1046733
Supporting Variants
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)nssv3697551
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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