A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556051



Internal ID16343460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99182486..99236286hg38UCSC Ensembl
Innerchr11:99053217..99107017hg19UCSC Ensembl
Innerchr11:98558427..98612227hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3853801
hg1953801
hg1853801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781724
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556051
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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