A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1297n145



Internal ID22814313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22208832..22739725hg38UCSC Ensembl
chrY:24354979..24885872hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38530894
hg19530894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117899, nsv3111880
Samplessample66, sample136
Known GenesLOC100652931, PRY, PRY2, RBMY1F, RBMY1J, RBMY2FP, TTTY5, TTTY6, TTTY6B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1297n145
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