A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220455



Internal ID22365145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37473088..37473197hg38UCSC Ensembl
chr9:37473085..37473194hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346502, nssv14346501, nssv14346503
SamplesNA19238, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220455
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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