A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15707023



Internal ID21379299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10507911..10507961hg38UCSC Ensembl
chr3:10549595..10549645hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390328
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15707023
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.272989


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