A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14279984



Internal ID22262996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:144650327..144691839hg38UCSC Ensembl
Outerchr8:145875712..145917224hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383081
hg193081
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243919
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14279984
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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