A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520203



Internal ID296537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5854587..5860418hg38UCSC Ensembl
chr18:5854586..5860417hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385832
hg195832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520203
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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