A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555185



Internal ID15995908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64174262..64322402hg38UCSC Ensembl
Innerchr11:63941734..64089874hg19UCSC Ensembl
Innerchr11:63698310..63846450hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38148141
hg19148141
hg18148141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1963n54
Supporting Variantsnssv777148
Samples
Known GenesBAD, DNAJC4, ESRRA, FERMT3, FKBP2, GPR137, KCNK4, NUDT22, PLCB3, PPP1R14B, PRDX5, STIP1, TEX40, TRMT112, TRPT1, VEGFB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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