A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182921



Internal ID20749961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78025860..78042193hg38UCSC Ensembl
chr16:78059757..78076090hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3816334
hg1916334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504529
Supporting Variants
Samples
Known GenesCLEC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182921
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00087


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