A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101113



Internal ID21444155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3288683..3288683hg38UCSC Ensembl
chr18:3288681..3288681hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663468
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101113
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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