A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526532



Internal ID22395912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87451198..87451656hg38UCSC Ensembl
chr1:87916881..87917339hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375840, nssv14383188
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526532
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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