A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467759



Internal ID245569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88306803..88309055hg38UCSC Ensembl
chr5:87602620..87604872hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382253
hg192253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968839
Samples
Known GenesTMEM161B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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