A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658652



Internal ID9578071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88949359..88949811hg38UCSC Ensembl
chr16:89015767..89016219hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6595278, essv6020712, essv5806885
SamplesNA18507, NA18912, NA19130
Known GenesCBFA2T3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658652
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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