A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089038



Internal ID21290820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127345042..127351184hg38UCSC Ensembl
Innerchr10:129143306..129149448hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg386143
hg196143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110891
Supporting Variants
Samplessample65
Known GenesDOCK1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089038
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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