A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225762



Internal ID22368795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65842768..65843041hg38UCSC Ensembl
chr11:65610239..65610512hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360483
SamplesHG00513
Known GenesSNX32
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225762
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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