A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546738



Internal ID320653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35434238..35434238hg38UCSC Ensembl
chr11:35455786..35455786hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044230
Samples
Known GenesPAMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546738
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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