A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6157018



Internal ID8808588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18197351..18198516hg38UCSC Ensembl
chr20:18177995..18179160hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662523
Supporting Variants
SamplesHG00253
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6157018
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