A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555371



Internal ID16342780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70137288..70142028hg38UCSC Ensembl
Innerchr11:69983394..69988134hg19UCSC Ensembl
Innerchr11:69661042..69665782hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg384741
hg194741
hg184741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1997n54
Supporting Variantsnssv778905
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555371
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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