A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118236



Internal ID21301502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68228058..68235665hg38UCSC Ensembl
Innerchr10:69987815..69995422hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387608
hg197608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088747
Samplessample296
Known GenesATOH7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118236
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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