A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14306414



Internal ID22165736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22437008..22446124hg38UCSC Ensembl
chr3:22478499..22487615hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg389117
hg199117
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209715
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14306414
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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