A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5678606



Internal ID9088016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54814725..54825499hg38UCSC Ensembl
chr5:54110553..54121327hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3810775
hg1910775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662816
Supporting Variants
SamplesHG01069
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5678606
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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