A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209580



Internal ID20776620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134413025..134444055hg38UCSC Ensembl
chr3:134131867..134162897hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3831031
hg1931031
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363493
Supporting Variants
Samples
Known GenesMIR4788
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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