A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160077



Internal ID21413120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125557649..125557649hg38UCSC Ensembl
chr9:128319928..128319928hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626902
Supporting Variants
SamplesHG00513
Known GenesMAPKAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160077
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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