A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14266889



Internal ID22135326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:801390..853079hg38UCSC Ensembl
Outerchr20:782033..833722hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3239739
Supporting Variants
SamplesHG00513
Known GenesFAM110A
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14266889
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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