A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671794



Internal ID9937899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2937752..2962844hg38UCSC Ensembl
chr16:2987753..3012845hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3825093
hg1925093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5508938
SamplesNA20802
Known GenesFLYWCH1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671794
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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