A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039196



Internal ID93864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114205124..114205175hg38UCSC Ensembl
chr10:115964883..115964934hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409223
Supporting Variants
Samples
Known GenesTDRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039196
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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