A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8944022



Internal ID14826164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21699267..21699357hg38UCSC Ensembl
Innerchr9:21699292..21699329hg38UCSC Ensembl
Outerchr9:21699242..21699382hg38UCSC Ensembl
chr9:21699266..21699356hg19UCSC Ensembl
Innerchr9:21699291..21699328hg19UCSC Ensembl
Outerchr9:21699241..21699381hg19UCSC Ensembl
chr9:21689266..21689356hg18UCSC Ensembl
Innerchr9:21689291..21689328hg18UCSC Ensembl
Outerchr9:21689241..21689381hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38131
hg19131
hg18131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3358434
Supporting Variants
SamplesNA19099
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8944022
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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