A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226619



Internal ID22369358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23849600..23850153hg38UCSC Ensembl
chr9:23849598..23850151hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14345886
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226619
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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