A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217045



Internal ID22362834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134182792..134182940hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347889, nssv14347888
SamplesHG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217045
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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