A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14284064



Internal ID22127657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48005643..48006152hg38UCSC Ensembl
chr18:45532014..45532523hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221861
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14284064
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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