A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490568



Internal ID267822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130109075..130159190hg38UCSC Ensembl
chr9:132871354..132921469hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3850116
hg1950116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028146
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490568
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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