A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208686



Internal ID20775728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71130830..71734979hg38UCSC Ensembl
chr3:71179981..71784130hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38604150
hg19604150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365532
Supporting Variants
Samples
Known GenesEIF4E3, FOXP1, MIR1284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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