A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215265



Internal ID22361659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60047166..60064658hg38UCSC Ensembl
chr16:60081070..60098562hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3817493
hg1917493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386683
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215265
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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