A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360501



Internal ID22284879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66166427..66171848hg38UCSC Ensembl
chr11:65933898..65939319hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385422
hg195422
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528103
Supporting Variants
SamplesNA19239
Known GenesPACS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360501
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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