A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218597



Internal ID22363890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62009713..62010573hg38UCSC Ensembl
chr11:61777185..61778045hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359729
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218597
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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