A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533334



Internal ID309225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57887616..57888025hg38UCSC Ensembl
chr17:55964977..55965386hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713781
Samples
Known GenesCUEDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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