A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435453



Internal ID214098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161584798..161585380hg38UCSC Ensembl
chr2:162441308..162441890hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16920259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435453
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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