A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555332



Internal ID16342741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70133454..70137396hg38UCSC Ensembl
Innerchr11:69979560..69983502hg19UCSC Ensembl
Innerchr11:69657208..69661150hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg383943
hg193943
hg183943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1992n54
Supporting Variantsnssv778765
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555332
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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