A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528881



Internal ID304922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45819953..45820007hg38UCSC Ensembl
chr18:43399918..43399972hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528881
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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