A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128999



Internal ID21497841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39575788..39575788hg38UCSC Ensembl
chr3:39617279..39617279hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg382145
hg192145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618551
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128999
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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