A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215392



Internal ID22361741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131295396..131295530hg38UCSC Ensembl
chr11:131165291..131165425hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362955, nssv14362956, nssv14362957
SamplesNA19239, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215392
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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