A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218205



Internal ID22363622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16104090..16104216hg38UCSC Ensembl
chr19:16214900..16215026hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286215, nssv14286217, nssv14286220, nssv14286218, nssv14286214, nssv14286219, nssv14286216
SamplesNA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218205
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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