A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110176



Internal ID21293442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:42625781..42633491hg38UCSC Ensembl
Innerchr12:43019583..43027293hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg387711
hg197711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv255n145
Supporting Variantsnssv14093799, nssv14091258
Samplessample366, sample190
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110176
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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