A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111688



Internal ID21294954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91219861..91222685hg38UCSC Ensembl
Innerchr10:92979618..92982442hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg382825
hg192825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089804
Samplessample348
Known GenesPCGF5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111688
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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