A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222998



Internal ID20790038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67363586..67439342hg38UCSC Ensembl
chr8:68275821..68351577hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3875757
hg1975757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432872
Supporting Variants
Samples
Known GenesCPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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