A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115798



Internal ID21299064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210268206..210272182hg38UCSC Ensembl
Innerchr1:210441551..210445527hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg383977
hg193977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093228
Samplessample283
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115798
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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