A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199339



Internal ID22348936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145289786..145394078hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38104293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285191, nssv14285190, nssv14285194, nssv14285188, nssv14285193, nssv14285192, nssv14285189, nssv14285187, nssv14285186
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199339
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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