A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229139



Internal ID20796179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86690401..86698200hg38UCSC Ensembl
chr8:87702629..87710428hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427065
Supporting Variants
Samples
Known GenesCNGB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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