A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555666



Internal ID16343075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86571638..86575355hg38UCSC Ensembl
Innerchr11:86282680..86286397hg19UCSC Ensembl
Innerchr11:85960328..85964045hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383718
hg193718
hg183718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2046n54
Supporting Variantsnssv779962, nssv779960, nssv779961
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555666
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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