A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116132



Internal ID21299398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35037064..35039389hg38UCSC Ensembl
Innerchr1:35502665..35504990hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382326
hg192326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088179
Samplessample234
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116132
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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