A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218549



Internal ID20785589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23029981..23202291hg38UCSC Ensembl
chr8:22887494..23059804hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38172311
hg19172311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417198
Supporting Variants
Samples
Known GenesLOC254896, LOC286059, TNFRSF10A, TNFRSF10B, TNFRSF10C, TNFRSF10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218549
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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