A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5680260



Internal ID9585666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100420061..100420563hg38UCSC Ensembl
chr10:102179818..102180320hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669151
Supporting Variants
SamplesNA19190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5680260
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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