A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559963



Internal ID22428758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51070888..51070888hg38UCSC Ensembl
chr13:51645024..51645024hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368454, nssv14368452, nssv14368458, nssv14368457, nssv14368451, nssv14368456, nssv14368455, nssv14368453, nssv14368450
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)nsv3559963
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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