A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485071



Internal ID262468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92558928..92575348hg38UCSC Ensembl
chr9:95321210..95337630hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3816421
hg1916421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027422
Samples
Known GenesCENPP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485071
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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