A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6279447



Internal ID9319408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26053317..26053677hg38UCSC Ensembl
chr18:23633281..23633641hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674101
Supporting Variants
SamplesNA18510
Known GenesSS18
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6279447
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