A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3304105



Internal ID15151053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89224967..89224968hg38UCSC Ensembl
Innerchr16:89224945..89224990hg38UCSC Ensembl
Outerchr16:89224944..89224991hg38UCSC Ensembl
chr16:89291375..89291376hg19UCSC Ensembl
Innerchr16:89291353..89291398hg19UCSC Ensembl
Outerchr16:89291352..89291399hg19UCSC Ensembl
chr16:87818876..87818877hg18UCSC Ensembl
Innerchr16:87818899..87818854hg18UCSC Ensembl
Outerchr16:87818853..87818900hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38291
hg19291
hg18291
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7765081, essv7768411, essv7763501, essv7766461, essv7764346, essv7767578, essv7766933, essv7769011, essv7766185, essv7769439
SamplesNA19141, NA12814, NA12812, NA07347, NA12287, NA18970, NA12872, NA11881, NA12873, NA12874
Known GenesZNF778
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3304105
Frequency
Sample Size185
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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