A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555707



Internal ID15996430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87083814..87274539hg38UCSC Ensembl
Innerchr11:86794856..86985581hg19UCSC Ensembl
Innerchr11:86472504..86663229hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38190726
hg19190726
hg18190726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780238
Samples
Known GenesTMEM135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555707
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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