A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357516



Internal ID22210560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45111212..45111405hg38UCSC Ensembl
chr11:45132763..45132956hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529403
Supporting Variants
SamplesHG00732
Known GenesPRDM11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357516
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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