A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098624



Internal ID21285637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12019930..12024784hg38UCSC Ensembl
Innerchr17:11923247..11928101hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384855
hg194855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115306
Supporting Variants
Samplessample378
Known GenesMAP2K4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098624
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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