A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14449402



Internal ID22221910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23653657..23654014hg38UCSC Ensembl
chr20:23634294..23634651hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205600
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14449402
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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