A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14297611



Internal ID22272389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20827744..20827980hg38UCSC Ensembl
chr20:20808387..20808623hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217615
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14297611
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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