A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111277



Internal ID21294543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28293748..28312758hg38UCSC Ensembl
Innerchr10:28582677..28601687hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3819011
hg1919011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088948
Samplessample20
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111277
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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