A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189760



Internal ID20756800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28265748..28318656hg38UCSC Ensembl
chr16:28277069..28329977hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3852909
hg1952909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507555
Supporting Variants
Samples
Known GenesSBK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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