A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210471



Internal ID20777511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27528116..27598254hg38UCSC Ensembl
chr3:27569607..27639745hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3870139
hg1970139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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