A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223654



Internal ID22367352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:38453665..38632241hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38178577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv881n152
Supporting Variantsnssv14280509
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223654
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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