A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089076



Internal ID21292289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127345396..127348844hg38UCSC Ensembl
Innerchr10:129143660..129147108hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383449
hg193449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116536
Supporting Variants
Samplessample86
Known GenesDOCK1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089076
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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