A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526566



Internal ID22395946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141272528..141272704hg38UCSC Ensembl
chr3:140991370..140991546hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309556, nssv14309555, nssv14309552, nssv14309554, nssv14309553
SamplesNA19238, NA19239, HG00731, HG00732, NA19240
Known GenesACPL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526566
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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