A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118104



Internal ID21301370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45000185..45001983hg38UCSC Ensembl
Innerchr10:45495633..45497431hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381799
hg191799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088730
Samplessample289
Known GenesC10orf25, ZNF22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118104
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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