A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221108



Internal ID22365604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89734770..89735099hg38UCSC Ensembl
chr15:90278001..90278330hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375993, nssv14387392
SamplesHG00732, HG00513
Known GenesWDR93
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221108
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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