A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205600



Internal ID22354270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23653657..23654014hg38UCSC Ensembl
chr20:23634294..23634651hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14449402
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)nsv3205600
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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