A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088509



Internal ID21272324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76271650..76385282hg38UCSC Ensembl
Innerchr10:78031408..78145040hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38113633
hg19113633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114527
Supporting Variants
Samplessample176
Known GenesC10orf11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088509
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer