A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360800



Internal ID22253136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107590331..107590445hg38UCSC Ensembl
chr11:107461057..107461171hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210686
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360800
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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