A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128940



Internal ID21410560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107391272..107391272hg38UCSC Ensembl
chr3:107110119..107110119hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622200
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128940
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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