A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305264



Internal ID15152212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21699265..21699266hg38UCSC Ensembl
Innerchr9:21699208..21699323hg38UCSC Ensembl
Outerchr9:21699207..21699324hg38UCSC Ensembl
chr9:21699264..21699265hg19UCSC Ensembl
Innerchr9:21699207..21699322hg19UCSC Ensembl
Outerchr9:21699206..21699323hg19UCSC Ensembl
chr9:21689264..21689265hg18UCSC Ensembl
Innerchr9:21689322..21689207hg18UCSC Ensembl
Outerchr9:21689206..21689323hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38131
hg19131
hg18131
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7752653
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305264
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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