A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111884



Internal ID21295150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:91220524..91224565hg38UCSC Ensembl
Innerchr12:91614301..91618342hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg384042
hg194042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093291
Samplessample423
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111884
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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