A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100031



Internal ID20667071
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 StatusS
Merged Variantsnsv6362466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00109


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