A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv870n145



Internal ID22813886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26858768..26862914hg38UCSC Ensembl
chr4:26860390..26864536hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384147
hg194147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110269, nsv3111041
Samplessample348, sample139
Known GenesSTIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv870n145
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