A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602225



Internal ID21550882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106977212..106979770hg38UCSC Ensembl
chr9:109739493..109742051hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146210
SamplesNA19238
Known GenesMIR548Q, ZNF462
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602225
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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