A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089050



Internal ID21291379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11609952..11612496hg38UCSC Ensembl
Innerchr10:11651951..11654495hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382545
hg192545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110156
Supporting Variants
Samplessample72
Known GenesUSP6NL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089050
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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