A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359726



Internal ID22143325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61982725..61983020hg38UCSC Ensembl
chr11:61750197..61750492hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223252
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359726
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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