A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv405n71



Internal ID6318025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169538466..169547610hg19UCSC Ensembl
chr1:167805090..167814234hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv872536, nsv872537
SamplesSP54442, SP52708
Known GenesF5
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv405n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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