A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037643



Internal ID92847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101736343..101736405hg38UCSC Ensembl
chr10:103496100..103496162hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143308
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037643
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003453


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