A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521101



Internal ID18472696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90286291..90501348hg38UCSC Ensembl
Innerchr11:90019459..90234516hg19UCSC Ensembl
Innerchr11:89659107..89874164hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38215058
hg19215058
hg18215058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053917
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521101
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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