A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210555



Internal ID20777595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3472098..3500100hg38UCSC Ensembl
chr3:3513782..3541784hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3828003
hg1928003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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