A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703270



Internal ID21375546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152453505..152453569hg38UCSC Ensembl
chr4:153374657..153374721hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391531
Supporting Variants
Samples
Known GenesFBXW7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703270
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0488506


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