A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14432726



Internal ID22175621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64172573..64177466hg38UCSC Ensembl
chr20:62803926..62808819hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384894
hg194894
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193481
Supporting Variants
SamplesHG00514
Known GenesMYT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14432726
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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