A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172698



Internal ID20739738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86412101..86866200hg38UCSC Ensembl
chr8:87424330..87878428hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38454100
hg19454099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429490
Supporting Variants
Samples
Known GenesCNGB3, CPNE3, RMDN1, WWP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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