A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556126



Internal ID16343535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100238133..100263565hg38UCSC Ensembl
Innerchr11:100108865..100134297hg19UCSC Ensembl
Innerchr11:99614075..99639507hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3825433
hg1925433
hg1825433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781992
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556126
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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