A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100174



Internal ID21280362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5887753..5894457hg38UCSC Ensembl
Innerchr18:5887752..5894456hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386705
hg196705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116897
Supporting Variants
Samplessample296
Known GenesTMEM200C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100174
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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