A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506648



Internal ID20879932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53964001..53966100hg38UCSC Ensembl
chr16:53997913..54000012hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030113
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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