A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170255



Internal ID20737295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86525025..86528074hg38UCSC Ensembl
chr8:87537253..87540302hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383050
hg193050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431127
Supporting Variants
Samples
Known GenesCPNE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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