A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119861



Internal ID21451622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81977471..81977471hg38UCSC Ensembl
chr3:82026622..82026622hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3834276
hg1934276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612531
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119861
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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