A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201665



Internal ID22350933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133516230..133516682hg38UCSC Ensembl
chr3:133235074..133235526hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308764
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201665
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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