A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542459



Internal ID316876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10764901..10764952hg38UCSC Ensembl
chr11:10786448..10786499hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043291
Samples
Known GenesCTR9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542459
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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