A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126130



Internal ID21452774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71991362..71991362hg38UCSC Ensembl
chr3:72040513..72040513hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608160
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126130
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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