A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705840



Internal ID21378116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101923806..101923927hg38UCSC Ensembl
chr14:102390143..102390264hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391214
Supporting Variants
Samples
Known GenesPPP2R5C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705840
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0143678


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