A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226339



Internal ID22369174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39418524..39430501hg38UCSC Ensembl
chr9:39418521..39430498hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3811978
hg1911978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347252, nssv14347251, nssv14347245, nssv14347253, nssv14347249, nssv14347247, nssv14347248, nssv14347246, nssv14347250
SamplesHG00512, NA19238, 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)nsv3226339
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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