A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114677



Internal ID21297943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151248884..151253264hg38UCSC Ensembl
Innerchr3:150966672..150971052hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg384381
hg194381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107037
Samplessample253
Known GenesMED12L, P2RY14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114677
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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