A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220947



Internal ID20787987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137769559..138242237hg38UCSC Ensembl
chr8:138781802..139254480hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38472679
hg19472679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419615
Supporting Variants
Samples
Known GenesFAM135B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220947
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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