A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089794



Internal ID21283378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132808145..132889939hg38UCSC Ensembl
Innerchr10:134621649..134703443hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3881795
hg1981795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110354
Supporting Variants
Samplessample343
Known GenesTTC40
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089794
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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