A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114034



Internal ID21297300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12019930..12022852hg38UCSC Ensembl
Innerchr17:11923247..11926169hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382923
hg192923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098578, nssv14097672
Samplessample224, sample361
Known GenesMAP2K4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114034
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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