A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529299



Internal ID22398692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58235905..58236019hg38UCSC Ensembl
chr11:58003377..58003491hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358903, nssv14358904
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529299
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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