A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560454



Internal ID22429251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49652608..49652608hg38UCSC Ensembl
chr15:49944805..49944805hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387769, nssv14379062
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560454
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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