A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555881



Internal ID16343290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90673352..90739547hg38UCSC Ensembl
Innerchr11:90406520..90472715hg19UCSC Ensembl
Innerchr11:90046168..90112363hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3866196
hg1966196
hg1866196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780812
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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