A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215150



Internal ID22361578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54544098..54551629hg38UCSC Ensembl
chr16:54578010..54585541hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg387532
hg197532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14384667
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215150
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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