A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6524372



Internal ID9501775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34654026..34656451hg38UCSC Ensembl
chr20:33241830..33244255hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672886
Supporting Variants
SamplesNA12144
Known GenesPIGU
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6524372
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