A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099042



Internal ID21268057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2607648..2614944hg38UCSC Ensembl
Innerchr20:2588294..2595590hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387297
hg197297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111575
Supporting Variants
Samplessample12
Known GenesTMC2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099042
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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