A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3541652



Internal ID22410744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35564372..35564521hg38UCSC Ensembl
chr20:34152140..34152438hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38150
hg19299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299964, nssv14299965, nssv14299963
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3541652
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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