A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14298670



Internal ID22261011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10323921..10324065hg38UCSC Ensembl
chr20:10304569..10304713hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3533508
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14298670
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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