A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123406



Internal ID21500914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39571478..39571478hg38UCSC Ensembl
chr3:39612969..39612969hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608843
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123406
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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