A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555235



Internal ID16342644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944941..66945426hg38UCSC Ensembl
Innerchr11:66712412..66712897hg19UCSC Ensembl
Innerchr11:66468988..66469473hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38486
hg19486
hg18486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1972n54
Supporting Variantsnssv778542, nssv778543
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555235
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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