A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660591



Internal ID9580010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25054809..25125941hg38UCSC Ensembl
Outerchr16:25054775..25125976hg38UCSC Ensembl
Innerchr16:25066130..25137262hg19UCSC Ensembl
Outerchr16:25066096..25137297hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3871202
hg1971202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5549388
SamplesHG00359
Known GenesLCMT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660591
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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