A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210427



Internal ID20777467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23327004..23676760hg38UCSC Ensembl
chr3:23368495..23718251hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38349757
hg19349757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373205
Supporting Variants
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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