A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225990



Internal ID22368947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113285255..113285666hg38UCSC Ensembl
chr9:116047535..116047946hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349096
SamplesNA19238
Known GenesPRPF4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225990
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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