A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112410



Internal ID21295676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13571254..13575490hg38UCSC Ensembl
Innerchr9:13571253..13575489hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384237
hg194237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1220n145
Supporting Variantsnssv14088079, nssv14088067, nssv14087870, nssv14089668, nssv14090767, nssv14090805, nssv14089507, nssv14087904, nssv14087897, nssv14088011, nssv14089741, nssv14089710, nssv14088870, nssv14088844, nssv14088404, nssv14088883, nssv14088896
Samplessample322, sample167, sample420, sample156, sample125, sample400, sample143, sample58, sample414, sample291, sample186, sample5, sample424, sample233, sample243, sample318, sample246
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112410
Frequency
Sample Size467
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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