A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555685



Internal ID16343094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86592284..86595333hg38UCSC Ensembl
Innerchr11:86303326..86306375hg19UCSC Ensembl
Innerchr11:85980974..85984023hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383050
hg193050
hg183050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780102
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555685
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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