A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529123



Internal ID22398516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68133672..68136589hg38UCSC Ensembl
chr15:68426010..68428927hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382918
hg192918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2967n152
Supporting Variantsnssv14376340, nssv14388958, nssv14381536, nssv14391493, nssv14376304, nssv14381245, nssv14378343, nssv14379622, nssv14382548
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesPIAS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529123
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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