A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634076



Internal ID21582381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129127307..129127307hg38UCSC Ensembl
chr9:131889586..131889586hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160315
SamplesHG03371
Known GenesPPP2R4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634076
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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