A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3362327



Internal ID15209305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32180630..32187128hg38UCSC Ensembl
Innerchr16:32181630..32186128hg38UCSC Ensembl
Outerchr16:32179630..32188128hg38UCSC Ensembl
chr16:32191951..32198449hg19UCSC Ensembl
Innerchr16:32192951..32197449hg19UCSC Ensembl
Outerchr16:32190951..32199449hg19UCSC Ensembl
chr16:32099452..32105950hg18UCSC Ensembl
Innerchr16:32100452..32104950hg18UCSC Ensembl
Outerchr16:32098452..32106950hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg386499
hg196499
hg186499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689988
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3362327
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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