A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086059



Internal ID21491043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39519562..39519562hg38UCSC Ensembl
chr15:39811763..39811763hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653515
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086059
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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