A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391716



Internal ID22449586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129530533..129530533hg38UCSC Ensembl
chr3:129249376..129249376hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951882
Supporting Variants
Samples
Known GenesRHO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391716
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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