A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228755



Internal ID22370836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142241763..142242389hg38UCSC Ensembl
chr8:143323124..143323750hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343555
SamplesNA19238
Known GenesTSNARE1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228755
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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