A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224161



Internal ID22367677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112457232..112460327hg38UCSC Ensembl
chr9:115219512..115222607hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383096
hg193096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349073, nssv14349069, nssv14349067, nssv14349070, nssv14349066, nssv14349068, nssv14349072, nssv14349065, nssv14349071
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesHSDL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224161
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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