A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489877



Internal ID267147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:663905..664045hg38UCSC Ensembl
chr10:709845..709985hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030851
Samples
Known GenesDIP2C, PRR26
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489877
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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