A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039421



Internal ID93997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100734580..100734655hg38UCSC Ensembl
chr10:102494337..102494412hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039421
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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