A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553756



Internal ID16341165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23316168..23423241hg38UCSC Ensembl
Innerchr11:23337714..23444787hg19UCSC Ensembl
Innerchr11:23294290..23401363hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38107074
hg19107074
hg18107074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768953
Samples
Known GenesMIR8054
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553756
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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