A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560595



Internal ID22429393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98437709..98437709hg38UCSC Ensembl
chr15:98980938..98980938hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380409, nssv14385319, nssv14388778, nssv14381992, nssv14386216, nssv14373262, nssv14387090
SamplesHG00512, NA19238, NA19239, HG00731, HG00733, HG00513, HG00514
Known GenesFAM169B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560595
Frequency
Sample Size9
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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