A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090199



Internal ID21481940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25620152..25620152hg38UCSC Ensembl
chr16:25631473..25631473hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658373
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090199
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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