A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080575



Internal ID21473142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24510342..24510342hg38UCSC Ensembl
chr16:24521663..24521663hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659094
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080575
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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