A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362466



Internal ID21020019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33101301..33107100hg38UCSC Ensembl
chr3:33142793..33148592hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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