A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561040



Internal ID22429833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59769208..59769208hg38UCSC Ensembl
chr15:60061407..60061407hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380637, nssv14389712, nssv14377870, nssv14391094, nssv14387667, nssv14382141, nssv14390524, nssv14382373
SamplesHG00512, 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)nsv3561040
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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