A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221351



Internal ID22365769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69325359..69325427hg38UCSC Ensembl
chr16:69359262..69359330hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14384621
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221351
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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