A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5398202



Internal ID177600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68767946..68767997hg38UCSC Ensembl
chr10:70527703..70527754hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035619
Samples
Known GenesCCAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5398202
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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