A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217945



Internal ID22363451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4310740..4311334hg38UCSC Ensembl
chr16:4360741..4361335hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392100, nssv14380277
SamplesNA19238, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217945
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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