A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111533



Internal ID21294799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114265297..114273595hg38UCSC Ensembl
Innerchr10:116025056..116033354hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg388299
hg198299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090126, nssv14090147
Samplessample122, sample133
Known GenesVWA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111533
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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