A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503620



Internal ID20876876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53830872..54123074hg38UCSC Ensembl
chr16:53864784..54156986hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38292203
hg19292203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030103
Samples
Known GenesFTO, FTO-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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