A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281471



Internal ID22254677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:93212770..93270483hg38UCSC Ensembl
Outerchr8:94224999..94282711hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3857714
hg1957713
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218361
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281471
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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