A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555660



Internal ID16343069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86180619..86194673hg38UCSC Ensembl
Innerchr11:85891661..85905715hg19UCSC Ensembl
Innerchr11:85569309..85583363hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3814055
hg1914055
hg1814055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779950
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555660
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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