A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039507



Internal ID94056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106566906..106569820hg38UCSC Ensembl
chr10:108326664..108329578hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382915
hg192915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039507
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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