A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929843



Internal ID22705102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53714810..53732556hg38UCSC Ensembl
chr16:53748722..53766468hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3817747
hg1917747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384277
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929843
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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