A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067763



Internal ID21480312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131949712..131949712hg38UCSC Ensembl
chr10:133763216..133763216hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632145
Supporting Variants
SamplesHG03683
Known GenesPPP2R2D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067763
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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