A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225533



Internal ID20792573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11026169..11026824hg38UCSC Ensembl
chr8:10883679..10884334hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421791
Supporting Variants
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.04449


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