A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361564



Internal ID22197644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113842640..113861211hg38UCSC Ensembl
chr11:113713362..113731933hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3818572
hg1918572
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216514
Supporting Variants
SamplesHG00732
Known GenesUSP28
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361564
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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