A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211542



Internal ID20778582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18247924..18252148hg38UCSC Ensembl
chr3:18289416..18293640hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384225
hg194225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367463
Supporting Variants
Samples
Known GenesLOC339862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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