A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226138



Internal ID22369050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3131857..3131909hg38UCSC Ensembl
chr11:3153087..3153139hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1243n152
Supporting Variantsnssv14357301, nssv14357299, nssv14357300
SamplesNA19238, NA19239, HG00733
Known GenesOSBPL5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226138
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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