A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098900



Internal ID21270187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22409331..22738178hg38UCSC Ensembl
Innerchr17:21908660..22237505hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38328848
hg19328846
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113451
Supporting Variants
Samplessample148
Known GenesFLJ36000, MTRNR2L1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098900
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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