A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7760084



Internal ID13784913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27823529..27823530hg38UCSC Ensembl
Innerchr9:27823496..27823563hg38UCSC Ensembl
Outerchr9:27823495..27823564hg38UCSC Ensembl
chr9:27823527..27823528hg19UCSC Ensembl
Innerchr9:27823494..27823561hg19UCSC Ensembl
Outerchr9:27823493..27823562hg19UCSC Ensembl
chr9:27813527..27813528hg18UCSC Ensembl
Innerchr9:27813561..27813494hg18UCSC Ensembl
Outerchr9:27813493..27813562hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38255
hg19255
hg18255
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307460
Supporting Variants
SamplesNA18501
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7760084
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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