A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555830



Internal ID15996553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90098215..90206280hg38UCSC Ensembl
Innerchr11:89831383..89939448hg19UCSC Ensembl
Innerchr11:89471031..89579096hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38108066
hg19108066
hg18108066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780542
Samples
Known GenesCHORDC1, NAALAD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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