A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3310464



Internal ID15157415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88625323..88627090hg38UCSC Ensembl
Outerchr9:88625323..88627090hg38UCSC Ensembl
Innerchr9:91240238..91242005hg19UCSC Ensembl
Outerchr9:91240238..91242005hg19UCSC Ensembl
Innerchr9:90431825..90430058hg18UCSC Ensembl
Outerchr9:90430058..90431825hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381066
hg191066
hg181066
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7843518
SamplesNA19240
Known Genes
MethodSequencing
Analysismapreads
PlatformABI SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3310464
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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