A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223165



Internal ID22367018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39471963..39477867hg38UCSC Ensembl
chr9:41616981..41622885hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385905
hg195905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347265, nssv14347266, nssv14347267, nssv14347263, nssv14347268, nssv14347271, nssv14347269, nssv14347264, nssv14347270
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)nsv3223165
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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