A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14268143



Internal ID22272236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:9591949..9641963hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3850015
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227367
Supporting Variants
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14268143
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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