A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357033



Internal ID22182324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68955251..68959100hg38UCSC Ensembl
chr11:68722720..68726569hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg383850
hg193850
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214186
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357033
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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