A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555706



Internal ID16343115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87077674..87115380hg38UCSC Ensembl
Innerchr11:86788716..86826422hg19UCSC Ensembl
Innerchr11:86466364..86504070hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3837707
hg1937707
hg1837707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176192
SamplesNINDS_223
Known GenesTMEM135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555706
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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