A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362529



Internal ID21020082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46244468..46246354hg38UCSC Ensembl
chr3:46285959..46287845hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381887
hg191887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209280
Samples
Known GenesCCR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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