A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5435n152



Internal ID22821138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9809749..9839479hg38UCSC Ensembl
chr4_gl000193_random:77063..106793hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3829731
hg1929731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3212151, nsv3225821
SamplesHG00512, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv5435n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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