A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362247



Internal ID22276971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128927173..128927599hg38UCSC Ensembl
chr11:128797068..128797494hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219331
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362247
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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