A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110603



Internal ID21293869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:150760953..150765230hg38UCSC Ensembl
Innerchr3:150478740..150483017hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg384278
hg194278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108169
Samplessample208
Known GenesSIAH2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110603
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