A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14395536



Internal ID22297276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43696981..43697485hg38UCSC Ensembl
chr20:42325621..42326125hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190774
Supporting Variants
SamplesNA19240
Known GenesMYBL2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14395536
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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