A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525013



Internal ID301191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41800472..41854020hg38UCSC Ensembl
chr18:39380437..39433985hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3853549
hg1953549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525013
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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