A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7752653



Internal ID15138520
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 StatusS
Merged Variantsesv3305264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7752653
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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