A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703973



Internal ID21376249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152972828..152972912hg38UCSC Ensembl
chr6:153293963..153294047hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392723
Supporting Variants
Samples
Known GenesFBXO5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703973
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0431034


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