A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040861



Internal ID94958
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 StatusS
Merged Variantsnsv5506164
Supporting Variants
Samples
Known GenesSFXN4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040861
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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