A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529884



Internal ID22399275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116500584..116500663hg38UCSC Ensembl
chr11:116371301..116371380hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360638
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529884
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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