A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299965



Internal ID22163083
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3541652
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299965
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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