A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090168



Internal ID21270048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22338807..22341723hg38UCSC Ensembl
Innerchr10:22627736..22630652hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg382917
hg192917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115308
Supporting Variants
Samplessample146
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090168
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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