A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439666



Internal ID218201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:59161363..59175835hg38UCSC Ensembl
chr2:59388498..59402970hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3814473
hg1914473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16914184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439666
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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