A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117559



Internal ID21300825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3896069..3898219hg38UCSC Ensembl
Innerchr10:3938261..3940411hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088721
Samplessample283
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117559
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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