A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216009



Internal ID20783049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167832304..167855580hg38UCSC Ensembl
chr5:167259309..167282585hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3823277
hg1923277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408731
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216009
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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