A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115591



Internal ID21298857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1360046..1365260hg38UCSC Ensembl
Innerchr10:1402241..1407455hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg385215
hg195215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088749
Samplessample299
Known GenesADARB2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115591
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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