A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110631



Internal ID21293897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39819111..39871253hg38UCSC Ensembl
Innerchr14:40288315..40340457hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3852143
hg1952143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096325
Samplessample278
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110631
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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