A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195849



Internal ID20762889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82726404..82755923hg38UCSC Ensembl
chr16:82760009..82789528hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3829520
hg1929520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501765
Supporting Variants
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195849
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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