A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208953



Internal ID20775993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13046372..13062743hg38UCSC Ensembl
chr3:13087872..13104243hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3816372
hg1916372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355744
Supporting Variants
Samples
Known GenesIQSEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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