A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213493



Internal ID22360422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130306601..130316100hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348532, nssv14348534, nssv14348530, nssv14348526, nssv14348533, nssv14348529, nssv14348527, nssv14348531, nssv14348528
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)nsv3213493
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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