A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559620



Internal ID332649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101034580..101034631hg38UCSC Ensembl
chr10:102794337..102794388hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg386015
hg196015
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039443
Samples
Known GenesSFXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559620
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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