A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200259



Internal ID22349738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32929581..32974979hg38UCSC Ensembl
Outerchr3:32971073..33016471hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3845399
hg1945399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270396
SamplesNA19238
Known GenesCCR4
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200259
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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