A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3309751



Internal ID15156702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89826797..89826798hg38UCSC Ensembl
Innerchr9:89826780..89826815hg38UCSC Ensembl
Outerchr9:89826779..89826816hg38UCSC Ensembl
chr9:92528244..92528245hg19UCSC Ensembl
Innerchr9:92528227..92528262hg19UCSC Ensembl
Outerchr9:92528226..92528263hg19UCSC Ensembl
chr9:91668064..91668065hg18UCSC Ensembl
Innerchr9:91668082..91668047hg18UCSC Ensembl
Outerchr9:91668046..91668083hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38173
hg19173
hg18173
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7841714, essv7842361
SamplesNA19238, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3309751
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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