A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223401



Internal ID20790441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43316434..43358885hg38UCSC Ensembl
chr6:43284172..43326623hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3842452
hg1942452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395962
Supporting Variants
Samples
Known GenesZNF318
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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