A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5886221



Internal ID9479160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25898943..25903170hg38UCSC Ensembl
chr10:26187872..26192099hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384228
hg194228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664215
Supporting Variants
SamplesNA18950
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5886221
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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