A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460096



Internal ID238093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34782119..34782284hg38UCSC Ensembl
chr5:34782224..34782389hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964224
Samples
Known GenesRAI14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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