A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220632



Internal ID22365279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63823164..63832040hg38UCSC Ensembl
chr11:63590636..63599512hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg388877
hg198877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359802
SamplesNA19239
Known GenesC11orf84
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220632
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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