A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521855



Internal ID298135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78397289..78397393hg38UCSC Ensembl
chr17:76393370..76393474hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714853
Samples
Known GenesPGS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521855
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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