A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527418



Internal ID22396804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104493269..104493375hg38UCSC Ensembl
chr9:107255550..107255656hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9698n152
Supporting Variantsnssv14347530, nssv14347533, nssv14347532, nssv14347531
SamplesNA19238, HG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527418
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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