A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115308



Internal ID21298574
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 StatusM
Merged Variants
Supporting Variantsnssv14090168
Samplessample146
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115308
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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