A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299890



Internal ID22295344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34200958..34201024hg38UCSC Ensembl
chr20:32788764..32788830hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3534748
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299890
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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