A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361350



Internal ID22115892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119486407..119486529hg38UCSC Ensembl
chr11:119357119..119357241hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220873
Supporting Variants
SamplesHG00512
Known GenesUSP2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361350
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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