A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704951



Internal ID21377227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103956120..103961010hg38UCSC Ensembl
chr10:105715878..105720768hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg384891
hg194891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389534
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704951
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0172414


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