A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496891



Internal ID20870094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69429540..69431628hg38UCSC Ensembl
chr16:69463443..69465531hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382089
hg192089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031795
Samples
Known GenesCYB5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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