A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176485



Internal ID15854799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115213585..115752165hg38UCSC Ensembl
Innerchr9:117975864..118514444hg19UCSC Ensembl
Innerchr9:117015685..117554265hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38538581
hg19538581
hg18538581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615251
Supporting Variants
Samples1780862339_A
Known GenesDEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176485
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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