A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466263



Internal ID244107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181096162..181169324hg38UCSC Ensembl
chr5:180523162..180596324hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3873163
hg1973163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978370
Samples
Known GenesOR2V1, OR2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466263
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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