A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088721



Internal ID21279475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3896069..3898219hg38UCSC Ensembl
Innerchr10:3938261..3940411hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117559
Supporting Variants
Samplessample283
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088721
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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