A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088967



Internal ID21282649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11609770..11612160hg38UCSC Ensembl
Innerchr10:11651769..11654159hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382391
hg192391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115860
Supporting Variants
Samplessample33
Known GenesUSP6NL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088967
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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