A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555183



Internal ID16342592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64039521..64077211hg38UCSC Ensembl
Innerchr11:63806993..63844683hg19UCSC Ensembl
Innerchr11:63563569..63601259hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3837691
hg1937691
hg1837691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777146
Samples
Known GenesMACROD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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