A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496672



Internal ID20869875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69455158..69455635hg38UCSC Ensembl
chr16:69489061..69489538hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031796
Samples
Known GenesCYB5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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