A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373205



Internal ID21030758
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 StatusM
Merged Variants
Supporting Variantsnssv18210427
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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