A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211288



Internal ID20778328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9824927..9830015hg38UCSC Ensembl
chr3:9866611..9871699hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg385089
hg195089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374783
Supporting Variants
Samples
Known GenesARPC4-TTLL3, TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211288
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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