A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116838



Internal ID21300104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17268159..17273264hg38UCSC Ensembl
Innerchr10:17310158..17315263hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg385106
hg195106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv144n145
Supporting Variantsnssv14088792, nssv14089083
Samplessample322, sample91
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116838
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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