A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089088



Internal ID21292892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6087667..6090717hg38UCSC Ensembl
Innerchr10:6129630..6132680hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383051
hg193051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110908
Supporting Variants
Samplessample93
Known GenesRBM17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089088
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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