A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110261



Internal ID21293527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:15434075..15450285hg38UCSC Ensembl
Innerchr12:15587009..15603219hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3816211
hg1916211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092784
Samplessample127
Known GenesPTPRO
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110261
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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