A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215929



Internal ID20782969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160273815..160275326hg38UCSC Ensembl
chr5:159700822..159702333hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381512
hg191512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415172
Supporting Variants
Samples
Known GenesCCNJL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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