A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225611



Internal ID22368686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53760227..53760641hg38UCSC Ensembl
chr16:53794139..53794553hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386094
SamplesHG00731
Known GenesFTO
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225611
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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