A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555348



Internal ID16342757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70136867..70147468hg38UCSC Ensembl
Innerchr11:69982973..69993574hg19UCSC Ensembl
Innerchr11:69660621..69671222hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3810602
hg1910602
hg1810602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1998n54
Supporting Variantsnssv778853
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555348
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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