A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477020



Internal ID254615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102618618..103011077hg38UCSC Ensembl
chr9:105380900..105773359hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38392460
hg19392460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026579
Samples
Known GenesCYLC2, LINC00587
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477020
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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