A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522231



Internal ID298502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34982051..34998607hg38UCSC Ensembl
chr18:32562015..32578571hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3816557
hg1916557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717281
Samples
Known GenesMAPRE2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522231
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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