A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361473



Internal ID22268716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123808260..123811091hg38UCSC Ensembl
chr11:123678968..123681799hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382832
hg192832
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211098
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361473
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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