A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461020



Internal ID238985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167025093..167064319hg38UCSC Ensembl
chr5:166452098..166491324hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3839227
hg1939227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461020
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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