A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229165



Internal ID22371098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:101630191..101637163hg38UCSC Ensembl
Outerchr10:103389948..103396920hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg386973
hg196973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278239, nssv14278240
SamplesNA19238, HG00513
Known GenesFBXW4
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229165
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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