A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485040



Internal ID262437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130084417..130084477hg38UCSC Ensembl
chr9:132846696..132846756hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028144
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485040
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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