A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv861n145



Internal ID22813877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17540842..17567600hg38UCSC Ensembl
chr4:17542465..17569223hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3826759
hg1926759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113119, nsv3113659, nsv3114574
Samplessample413, sample421, sample400, sample17, sample7, sample48, sample357, sample235, sample111, sample99
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv861n145
Frequency
Sample Size467
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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