A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3530008



Internal ID22399399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90819208..90819349hg38UCSC Ensembl
chr15:91362438..91362579hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3023n152
Supporting Variantsnssv14390364, nssv14377994, nssv14377137
SamplesHG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3530008
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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