A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552855



Internal ID15993578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:532923..545087hg38UCSC Ensembl
Innerchr11:532923..545087hg19UCSC Ensembl
Innerchr11:522923..535087hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3812165
hg1912165
hg1812165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763551
Samples
Known GenesHRAS, LRRC56
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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