A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562357



Internal ID22431111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43323464..43323464hg38UCSC Ensembl
chr20:41952104..41952104hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301427
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562357
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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