A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116053



Internal ID21299319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76733530..76739482hg38UCSC Ensembl
Innerchr17:74729612..74735564hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg385953
hg195953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098577
Samplessample360
Known GenesMETTL23, MFSD11, MIR636, SRSF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116053
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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