A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118177



Internal ID21301443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108679705..108682931hg38UCSC Ensembl
Innerchr1:109222327..109225553hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383227
hg193227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103804
Samplessample47
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118177
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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