A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527382



Internal ID22396768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128214384..128216760hg38UCSC Ensembl
chr11:128084279..128086655hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382377
hg192377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362203, nssv14362204
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527382
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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