A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555228



Internal ID15995951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66939371..66946955hg38UCSC Ensembl
Innerchr11:66706842..66714426hg19UCSC Ensembl
Innerchr11:66463418..66471002hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387585
hg197585
hg187585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778088
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555228
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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