A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223056



Internal ID22366938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83124211..83124589hg38UCSC Ensembl
chr11:82835253..82835631hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358724
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223056
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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