A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424421



Internal ID22482291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152804460..152804538hg38UCSC Ensembl
chr3:152522249..152522327hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424421
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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