A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053964



Internal ID18796495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:491334..692433hg38UCSC Ensembl
Innerchr11:491334..692433hg19UCSC Ensembl
Innerchr11:481334..682433hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38201100
hg19201100
hg18201100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706387
Samples
Known GenesC11orf35, CDHR5, DEAF1, DRD4, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, PTDSS2, RASSF7, RNH1, SCT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053964
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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