A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067762



Internal ID21446958
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 StatusS
Merged Variantsnsv5632145
Supporting Variants
SamplesHG00732
Known GenesPPP2R2D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067762
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer