A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361535



Internal ID22129804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110890743..110890797hg38UCSC Ensembl
chr11:110761467..110761521hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217477
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361535
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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