A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14395093



Internal ID22298672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63546516..63546582hg38UCSC Ensembl
chr20:62177869..62177935hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198866
Supporting Variants
SamplesNA19240
Known GenesSRMS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14395093
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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