A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100306



Internal ID21286593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31230016..31232034hg38UCSC Ensembl
Innerchr18:28809979..28811997hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg382019
hg192019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113943
Supporting Variants
Samplessample391
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100306
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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