A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618835



Internal ID21810882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54104464..54114377hg38UCSC Ensembl
chr16:54138376..54148289hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg389914
hg199914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040295
Supporting Variants
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618835
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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