A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5699455



Internal ID8676858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3568920..3571761hg38UCSC Ensembl
chr18:3568918..3571759hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382842
hg192842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660589
Supporting Variants
SamplesHG00443
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5699455
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