A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556565



Internal ID15997288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129996758..130180927hg38UCSC Ensembl
Innerchr11:129866653..130050822hg19UCSC Ensembl
Innerchr11:129371863..129556032hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38184170
hg19184170
hg18184170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785100
Samples
Known GenesAPLP2, LINC00167, PRDM10, ST14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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