A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112056



Internal ID21295322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66513966..66527034hg38UCSC Ensembl
Innerchr4:67379684..67392752hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3813069
hg1913069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv884n145
Supporting Variantsnssv14090397, nssv14107612
Samplessample87, sample138
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112056
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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