A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089807



Internal ID21283706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60999981..61002666hg38UCSC Ensembl
Innerchr10:62759739..62762424hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg382686
hg192686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118082
Supporting Variants
Samplessample349
Known GenesRHOBTB1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089807
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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