A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555880



Internal ID16343289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90577184..90628931hg38UCSC Ensembl
Innerchr11:90310352..90362099hg19UCSC Ensembl
Innerchr11:89950000..90001747hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3851748
hg1951748
hg1851748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780811
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555880
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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