A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302858



Internal ID15149806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26586816..26589300hg38UCSC Ensembl
Innerchr11:26586916..26589200hg38UCSC Ensembl
Outerchr11:26586716..26589400hg38UCSC Ensembl
chr11:26608363..26610847hg19UCSC Ensembl
Innerchr11:26608463..26610747hg19UCSC Ensembl
Outerchr11:26608263..26610947hg19UCSC Ensembl
chr11:26564939..26567423hg18UCSC Ensembl
Innerchr11:26565039..26567323hg18UCSC Ensembl
Outerchr11:26564839..26567523hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg382485
hg192485
hg182485
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7733576, essv7737291, essv7733532, essv7734333, essv7737986, essv7737525
SamplesNA07346, NA12287, NA12761, NA12003, NA07051, NA07000
Known GenesANO3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302858
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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