A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208920



Internal ID20775960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104197214..104201020hg38UCSC Ensembl
chr3:103916058..103919864hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg383807
hg193807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362541
Supporting Variants
Samples
Known GenesMIR548A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208920
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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