A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5460576



Internal ID8437979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89982475..89982547hg38UCSC Ensembl
Outerchr16:89982438..89982597hg38UCSC Ensembl
Innerchr16:90048883..90048955hg19UCSC Ensembl
Outerchr16:90048846..90049005hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664835
Supporting Variants
SamplesNA18547
Known GenesAFG3L1P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5460576
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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