A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231520



Internal ID20798560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86238020..86358293hg38UCSC Ensembl
chr8:87250249..87370522hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38120274
hg19120274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417698
Supporting Variants
Samples
Known GenesWWP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231520
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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