A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668353



Internal ID9934458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189506718..189507582hg38UCSC Ensembl
chr3:189224507..189225371hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6047132, essv6174925, essv5735743, essv5771113, essv5474661, essv5753659, essv6147609, essv5547939, essv5690308, essv5694695, essv5600462, essv6057761, essv5440188, essv5953068, essv5524182, essv5797816, essv5457150, essv6113060, essv5939722, essv6075591, essv6468918, essv5881280, essv6196081, essv5688395, essv5503490, essv5818132
SamplesHG01521, NA12286, NA20508, NA19914, NA20783, NA20507, NA18510, NA20806, HG01140, NA20774, NA12748, HG00108, NA10847, HG01197, HG01101, HG01075, HG00336, HG00638, NA20804, NA19248, NA19468, NA19780, HG01111, HG01125, NA12890, NA20754
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668353
Frequency
Sample Size1151
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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