A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221558



Internal ID22365902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92158105..92158232hg38UCSC Ensembl
chr11:91891271..91891398hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359374, nssv14359373
SamplesHG00731, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221558
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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