A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555704



Internal ID16343113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86633635..86675742hg38UCSC Ensembl
Innerchr11:86344677..86386784hg19UCSC Ensembl
Innerchr11:86022325..86064432hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3842108
hg1942108
hg1842108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780237
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555704
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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