A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089827



Internal ID21284698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91174952..91186731hg38UCSC Ensembl
Innerchr10:92934709..92946488hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3811780
hg1911780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116332
Supporting Variants
Samplessample364
Known GenesPCGF5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089827
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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