A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523544



Internal ID299772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69054483..69059175hg38UCSC Ensembl
chr16:69088386..69093078hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384693
hg194693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708528
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523544
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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