A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv780813



Internal ID16074769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90739547..90823189hg38UCSC Ensembl
Innerchr11:90472715..90556357hg19UCSC Ensembl
Innerchr11:90112363..90196005hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3883643
hg1983643
hg1883643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555882
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv780813
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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