A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415733



Internal ID22473603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86831757..86838503hg38UCSC Ensembl
chr3:86880907..86887653hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg386747
hg196747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415733
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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