A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115021



Internal ID21298287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:175184182..175195260hg38UCSC Ensembl
Innerchr1:175153318..175164396hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3811079
hg1911079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100465
Samplessample393
Known GenesKIAA0040
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115021
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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