A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542436



Internal ID316854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:110895595..110895595hg38UCSC Ensembl
chr3:110614442..110614442hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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