A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212968



Internal ID20780008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65405565..65411276hg38UCSC Ensembl
chr3:65391240..65396951hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385712
hg195712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357460
Supporting Variants
Samples
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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