A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232633



Internal ID20799673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:253801..453800hg38UCSC Ensembl
chr6:253801..453800hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38200000
hg19200000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412355
Supporting Variants
Samples
Known GenesDUSP22, IRF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5884


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