A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5597543



Internal ID8974133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89062370..89071323hg38UCSC Ensembl
chr10:90822127..90831080hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg388954
hg198954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665455
Supporting Variants
SamplesHG00554
Known GenesMIR4679-1, MIR4679-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5597543
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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