A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110611



Internal ID21293877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89489176..89492929hg38UCSC Ensembl
Innerchr10:91248933..91252686hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg383754
hg193754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089007
Samplessample52
Known GenesSLC16A12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110611
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