A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111303



Internal ID21294569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30084859..30090462hg38UCSC Ensembl
Innerchr12:30237792..30243395hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg385604
hg195604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv241n145
Supporting Variantsnssv14092569
Samplessample291
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111303
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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