A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029238



Internal ID87188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12237433..12237433hg38UCSC Ensembl
chr10:12279432..12279432hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551863
Supporting Variants
Samples
Known GenesCDC123
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029238
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010812


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer