A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479102



Internal ID256637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33472830..33510934hg38UCSC Ensembl
chr9:33472828..33510932hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3838105
hg1938105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023530
Samples
Known GenesNOL6, SUGT1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479102
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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