A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705877



Internal ID21378153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39567283..39567417hg38UCSC Ensembl
chr15:39859484..39859618hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391277
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705877
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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