A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432238



Internal ID21394240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60538802..60591801hg38UCSC Ensembl
chr15:60831001..60884000hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3853000
hg1953000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752512
SamplesSMI041
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432238
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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