A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv882n152



Internal ID22816585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38474632..38632372hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38157741
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3241291, nsv3233144, nsv3238150
SamplesHG00512, NA19238, NA19239, NA19240, HG00733, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv882n152
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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