A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205689



Internal ID22354350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64012519..64012575hg38UCSC Ensembl
chr20:62643872..62643928hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460257, nssv14409718
SamplesNA19240, HG00733
Known GenesPRPF6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205689
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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