A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632145



Internal ID21580450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131949712..131949712hg38UCSC Ensembl
chr10:133763216..133763216hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067762, nssv17067763
SamplesHG00732, HG03683
Known GenesPPP2R2D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632145
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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