A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555325



Internal ID16342734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69599509..69620462hg38UCSC Ensembl
Innerchr11:69414277..69435230hg19UCSC Ensembl
Innerchr11:69123458..69144411hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3820954
hg1920954
hg1820954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1991n54
Supporting Variantsnssv1174823
SamplesHGDP01001
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555325
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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