A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536138



Internal ID311681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163470731..163470731hg38UCSC Ensembl
chr2:164327241..164327241hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16926663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536138
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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