A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129260



Internal ID21507643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38704625..38704625hg38UCSC Ensembl
chr3:38746116..38746116hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618448
Supporting Variants
SamplesNA20509
Known GenesSCN10A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129260
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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