A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461350



Internal ID239304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171105000..171113750hg38UCSC Ensembl
chr5:170532004..170540754hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg388751
hg198751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977129
Samples
Known GenesRANBP17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461350
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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