A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154959



Internal ID22085464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89144598..89187161hg38UCSC Ensembl
Outerchr13:89144414..89193701hg38UCSC Ensembl
Innerchr13:89796852..89839415hg19UCSC Ensembl
Outerchr13:89796668..89845955hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3849288
hg1949288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008285, nssv4008288, nssv4008281, nssv4008278, nssv4008282, nssv4008283, nssv4008286, nssv4008287, nssv4008284, nssv4008280, nssv4008279
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154959
Frequency
Sample Size131
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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