A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3433321



Internal ID15280277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101866151..101866170hg38UCSC Ensembl
Innerchr11:101866147..101866174hg38UCSC Ensembl
Outerchr11:101866128..101866193hg38UCSC Ensembl
chr11:101736882..101736901hg19UCSC Ensembl
Innerchr11:101736878..101736905hg19UCSC Ensembl
Outerchr11:101736859..101736924hg19UCSC Ensembl
chr11:101242092..101242111hg18UCSC Ensembl
Innerchr11:101242115..101242088hg18UCSC Ensembl
Outerchr11:101242069..101242134hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9653803
SamplesNA12872
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3433321
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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