A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14297044



Internal ID22131995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1765950..1766087hg38UCSC Ensembl
chr20:1746596..1746733hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229546
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14297044
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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