A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223286



Internal ID22367105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:25814327..25828145hg38UCSC Ensembl
Outerchr14:26283533..26297351hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3813819
hg1913819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258918
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223286
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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