A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401170



Internal ID22459040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14548332..14569824hg38UCSC Ensembl
chr3:14589839..14611331hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3821493
hg1921493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905962
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401170
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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