A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211098



Internal ID22358769
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361473
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211098
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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