A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562133



Internal ID335092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22354630..22354681hg38UCSC Ensembl
chr10:22643559..22643610hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033733
Samples
Known GenesSPAG6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562133
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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