A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1147n209



Internal ID22827222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61808440..61825563hg38UCSC Ensembl
chr2:62035575..62052698hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3817124
hg1917124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5833083, nsv5833676
Samples
Known GenesFAM161A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1147n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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