A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537961



Internal ID313146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70211339..70211339hg38UCSC Ensembl
chr18:67878575..67878575hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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