A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372842



Internal ID21030395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33452009..33520957hg38UCSC Ensembl
chr3:33493501..33562449hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3868949
hg1968949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210540
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372842
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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