A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218253



Internal ID22363652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66624935..66625423hg38UCSC Ensembl
chr15:66917273..66917761hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383163
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218253
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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