A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114884



Internal ID21298150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61608822..61631986hg38UCSC Ensembl
Innerchr3:61594496..61617660hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3823165
hg1923165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107885
Samplessample294
Known GenesPTPRG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114884
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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