A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211291



Internal ID20778331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98494301..98810500hg38UCSC Ensembl
chr3:98213145..98529344hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38316200
hg19316200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368382
Supporting Variants
Samples
Known GenesCLDND1, CPOX, DCBLD2, GPR15, OR5K2, ST3GAL6, ST3GAL6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211291
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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