A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703566



Internal ID21375842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117358813..117359136hg38UCSC Ensembl
chr5:116694509..116694832hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392067
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703566
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0373563


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