A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561026



Internal ID22429820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63264905..63264905hg38UCSC Ensembl
chr18:60932138..60932138hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285605, nssv14285606, nssv14285601, nssv14285602, nssv14285604, nssv14285600, nssv14285599, nssv14285603, nssv14285598
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesBCL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561026
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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