A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555378



Internal ID16342787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70225821..70247989hg38UCSC Ensembl
Innerchr11:70071927..70094095hg19UCSC Ensembl
Innerchr11:69749575..69771743hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3822169
hg1922169
hg1822169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2000n54
Supporting Variantsnssv1174825
SamplesHGDP00520
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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