A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560120



Internal ID22428915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111611046..111611046hg38UCSC Ensembl
chr13:112263393..112263393hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369431, nssv14369433, nssv14369432
SamplesNA19239, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560120
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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