A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111927



Internal ID21295193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111571140..111575078hg38UCSC Ensembl
Innerchr5:110906837..110910775hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg383939
hg193939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096856, nssv14109097
Samplessample239, sample58
Known GenesSTARD4-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111927
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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