A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15707258



Internal ID21379534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149079464..149079517hg38UCSC Ensembl
chr3:148797251..148797304hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390750
Supporting Variants
Samples
Known GenesHLTF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15707258
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.41092


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