A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14280801



Internal ID22155396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:138223227..138240387hg38UCSC Ensembl
Outerchr9:141113677..141130837hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3247283
Supporting Variants
SamplesHG00514
Known GenesFAM157B
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14280801
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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