A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219331



Internal ID22364383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128927173..128927599hg38UCSC Ensembl
chr11:128797068..128797494hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362246, nssv14362244, nssv14362245, nssv14362243, nssv14362242, nssv14362248, nssv14362247, nssv14362241, nssv14362240
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219331
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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