A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211487



Internal ID20778527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17699715..17702365hg38UCSC Ensembl
chr3:17741207..17743857hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382651
hg192651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367805
Supporting Variants
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211487
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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