A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555484



Internal ID16342893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81606904..81652893hg38UCSC Ensembl
Innerchr11:81317946..81363935hg19UCSC Ensembl
Innerchr11:80995594..81041583hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3845990
hg1945990
hg1845990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174842
SamplesHGDP01029
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555484
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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