A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14278840



Internal ID22126631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:137098958..137119708hg38UCSC Ensembl
Outerchr8:138111201..138131951hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3820751
hg1920751
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213211
Supporting Variants
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14278840
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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