A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207905



Internal ID20774945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11905668..11907452hg38UCSC Ensembl
chr3:11947142..11948926hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg381785
hg191785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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