A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv881n152



Internal ID22816584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38453665..38632241hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38178577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3223654, nsv3228853
SamplesNA19238, HG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv881n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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