A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208578



Internal ID20775619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167102801..167142000hg38UCSC Ensembl
chr3:166820589..166859788hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839200
hg1939200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208578
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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