A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111820



Internal ID21295086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118416188..118419655hg38UCSC Ensembl
Innerchr10:120175700..120179167hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383468
hg193468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090145, nssv14089924, nssv14088562
Samplessample198, sample131, sample410
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111820
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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