A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454826



Internal ID22249360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20354477..20358913hg38UCSC Ensembl
chr20:20335121..20339557hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384437
hg194437
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205802
Supporting Variants
SamplesHG00733
Known GenesC20orf26
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454826
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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