A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489036



Internal ID266329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135634724..135634809hg38UCSC Ensembl
chr9:138526570..138526655hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031285
Samples
Known GenesGLT6D1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489036
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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