A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556053



Internal ID16343462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99193908..99255285hg38UCSC Ensembl
Innerchr11:99064639..99126016hg19UCSC Ensembl
Innerchr11:98569849..98631226hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3861378
hg1961378
hg1861378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2115n54
Supporting Variantsnssv781725
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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