A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527536



Internal ID22396923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118499447..118499577hg38UCSC Ensembl
chr11:118370162..118370292hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361332, nssv14361333
SamplesNA19238, NA19240
Known GenesKMT2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527536
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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