A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv266n97



Internal ID22815663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91397069..91417678hg38UCSC Ensembl
chr7:91026384..91046993hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3820610
hg1920610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156698, nsv1156696, nsv1156699, nsv1156700
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv266n97
Frequency
Sample Size131
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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