A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553267



Internal ID326532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35244912..35244952hg38UCSC Ensembl
chr17:33571931..33571971hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712800
Samples
Known GenesSLFN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553267
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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