A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552856



Internal ID15993579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:549119..619789hg38UCSC Ensembl
Innerchr11:549119..619789hg19UCSC Ensembl
Innerchr11:539119..609789hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3870671
hg1970671
hg1870671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763552
Samples
Known GenesC11orf35, CDHR5, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552856
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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