A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218903



Internal ID22364102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40509295..40512117hg38UCSC Ensembl
chr9:42844828..42847664hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg382823
hg192837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347325, nssv14347327, nssv14347328, nssv14347332, nssv14347326, nssv14347324, nssv14347331, nssv14347330, nssv14347329
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesLOC286297
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218903
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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