A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555227



Internal ID15995950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66939371..66945634hg38UCSC Ensembl
Innerchr11:66706842..66713105hg19UCSC Ensembl
Innerchr11:66463418..66469681hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386264
hg196264
hg186264
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778087, nssv778086
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555227
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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