A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209623



Internal ID20776663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139272416..139350546hg38UCSC Ensembl
chr3:138991258..139069388hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3878131
hg1978131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375098
Supporting Variants
Samples
Known GenesMRPS22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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