A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666619



Internal ID9586038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68004026..68045357hg38UCSC Ensembl
Outerchr16:68003989..68045407hg38UCSC Ensembl
Innerchr16:68037929..68079260hg19UCSC Ensembl
Outerchr16:68037892..68079310hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3841419
hg1941419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5466764
SamplesHG00437
Known GenesDDX28, DUS2, LOC100131303
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666619
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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