A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116913



Internal ID21300179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95839013..95843264hg38UCSC Ensembl
Innerchr12:96232791..96237042hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg384252
hg194252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv274n145
Supporting Variantsnssv14092924
Samplessample161
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116913
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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