A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660861



Internal ID9926966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82010102..82015982hg38UCSC Ensembl
chr16:82043707..82049587hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385881
hg195881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5671464, essv6560347
SamplesNA19675, NA19679
Known GenesSDR42E1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660861
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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