A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226891



Internal ID20793931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85437301..85475500hg38UCSC Ensembl
chr8:86349530..86387729hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3838200
hg1938200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423118
Supporting Variants
Samples
Known GenesCA2, CA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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