A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529538



Internal ID22398930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72209407..72209459hg38UCSC Ensembl
chr15:72501748..72501800hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2984n152
Supporting Variantsnssv14387222
SamplesNA19239
Known GenesPKM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529538
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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