A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485103



Internal ID262499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101368878..101371361hg38UCSC Ensembl
chr9:104131160..104133643hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382484
hg192484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026933
Samples
Known GenesBAAT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485103
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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