A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484333



Internal ID261746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90803893..90820638hg38UCSC Ensembl
chr10:92563650..92580395hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3816746
hg1916746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036857
Samples
Known GenesHTR7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484333
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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