A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552860



Internal ID15993583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:564295..636399hg38UCSC Ensembl
Innerchr11:564295..636399hg19UCSC Ensembl
Innerchr11:554295..626399hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3872105
hg1972105
hg1872105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1522n54
Supporting Variantsnssv763555
Samples
Known GenesCDHR5, IRF7, LOC143666, MIR210, MIR210HG, PHRF1, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552860
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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