A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113387



Internal ID21296653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17268159..17273542hg38UCSC Ensembl
Innerchr10:17310158..17315541hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg385384
hg195384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv144n145
Supporting Variantsnssv14090188, nssv14088739
Samplessample152, sample295
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113387
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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