A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522764



Internal ID299024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67579001..67590686hg38UCSC Ensembl
chr16:67612904..67624589hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3811686
hg1911686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707517
Samples
Known GenesCTCF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522764
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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