A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219263



Internal ID22364337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3717950..3718914hg38UCSC Ensembl
chr19:3717948..3718912hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291289
SamplesNA19239
Known GenesTJP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219263
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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