A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538676



Internal ID313735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45146845..45146867hg38UCSC Ensembl
chr11:45168396..45168418hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046159
Samples
Known GenesPRDM11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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