A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357117



Internal ID22142490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69784654..69784936hg38UCSC Ensembl
chr11:69599422..69599704hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529917
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357117
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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