A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv120n145



Internal ID22813136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234274308..234276827hg38UCSC Ensembl
chr1:234410054..234412573hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382520
hg192520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117465, nsv3115294
Samplessample304, sample92, sample207
Known GenesSLC35F3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv120n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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