A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471594



Internal ID22529486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53980956..53982105hg38UCSC Ensembl
chr16:54014868..54016017hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867775
Supporting Variants
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471594
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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