A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361343



Internal ID22115888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119290386..119290979hg38UCSC Ensembl
chr11:119161096..119161689hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226271
Supporting Variants
SamplesHG00512
Known GenesCBL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361343
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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