A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14297891



Internal ID22303328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6462475..6462574hg38UCSC Ensembl
chr20:6443122..6443221hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226869
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14297891
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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