A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535999



Internal ID311565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69409889..69409920hg38UCSC Ensembl
chr10:71169645..71169676hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035123
Samples
Known GenesTACR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535999
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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