A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560488



Internal ID22429285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96541061..96541061hg38UCSC Ensembl
chr15:97084291..97084291hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378198, nssv14383308, nssv14372795, nssv14375638
SamplesHG00512, NA19238, NA19239, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560488
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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