A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14406640



Internal ID22322086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20354584..20358945hg38UCSC Ensembl
chr20:20335228..20339589hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384362
hg194362
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190555
Supporting Variants
SamplesNA19240
Known GenesC20orf26
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14406640
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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