A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526692



Internal ID302813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62863310..62866484hg38UCSC Ensembl
chr18:60530543..60533717hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383175
hg193175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17718778
Samples
Known GenesPHLPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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