A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134125



Internal ID21497886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182277069..182277069hg38UCSC Ensembl
chr3:181994857..181994857hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619513
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134125
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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