A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7120n71



Internal ID6324740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2549111..2582584hg19UCSC Ensembl
chr7:2515637..2549110hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv887299, nsv887296
SamplesSP54988, SP54725
Known GenesBRAT1, LFNG, MIR4648
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv7120n71
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