A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661544



Internal ID9927649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:874758..881265hg38UCSC Ensembl
chr16:924758..931265hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386508
hg196508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5514371
SamplesNA19102
Known GenesLMF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661544
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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