A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504742



Internal ID281536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65821424..65841588hg38UCSC Ensembl
chr11:65588895..65609059hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3820165
hg1920165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046784
Samples
Known GenesSNX32
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504742
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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