A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529403



Internal ID22398795
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357514, nssv14357513, nssv14357515, nssv14357516, nssv14357512
SamplesHG00512, HG00731, HG00732, HG00513, HG00514
Known GenesPRDM11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529403
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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