A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146210



Internal ID21495969
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 StatusS
Merged Variantsnsv5602225
Supporting Variants
SamplesNA19238
Known GenesMIR548Q, ZNF462
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146210
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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