A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14300609



Internal ID22138221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36659669..36660156hg38UCSC Ensembl
chr20:35288072..35288559hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213869
Supporting Variants
SamplesHG00513
Known GenesNDRG3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14300609
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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