A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114027



Internal ID21297293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:45221414..45223897hg38UCSC Ensembl
Innerchr1:45687086..45689569hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382484
hg192484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109326
Samplessample149
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114027
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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