A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784646



Internal ID16078602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123648209..123666564hg38UCSC Ensembl
Innerchr11:123518917..123537272hg19UCSC Ensembl
Innerchr11:123024127..123042482hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3818356
hg1918356
hg1818356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556484
Supporting Variants
Samples
Known GenesSCN3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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