A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506164



Internal ID282917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119142065..119143180hg38UCSC Ensembl
chr10:120901577..120902692hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040861
Samples
Known GenesSFXN4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506164
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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