A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528663



Internal ID304711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57939186..57939499hg38UCSC Ensembl
chr17:56016547..56016860hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713784
Samples
Known GenesCUEDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528663
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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