A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112134



Internal ID21295400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17268695..17273542hg38UCSC Ensembl
Innerchr10:17310694..17315541hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384848
hg194848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv144n145
Supporting Variantsnssv14088635, nssv14088662, nssv14088788, nssv14088999, nssv14090089, nssv14088691, nssv14088554, nssv14088653, nssv14089849
Samplessample262, sample198, sample369, sample111, sample233, sample243, sample245, sample47, sample321
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112134
Frequency
Sample Size467
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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