A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6439581



Internal ID9416984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33496542..33498034hg38UCSC Ensembl
chr20:32084348..32085840hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381493
hg191493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660082
Supporting Variants
SamplesNA18502
Known GenesCBFA2T2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6439581
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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