A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229024



Internal ID20796064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123863301..123866200hg38UCSC Ensembl
chr8:124875541..124878440hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430185
Supporting Variants
Samples
Known GenesFER1L6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229024
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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