A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3451882



Internal ID15298827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62798833..62885306hg38UCSC Ensembl
Innerchr9:62799808..62884306hg38UCSC Ensembl
Outerchr9:62798833..62886306hg38UCSC Ensembl
chr9:66454657..66541130hg19UCSC Ensembl
Innerchr9:66455632..66540130hg19UCSC Ensembl
Outerchr9:66454657..66542130hg19UCSC Ensembl
chr9:66194452..66280950hg18UCSC Ensembl
Innerchr9:66195452..66279950hg18UCSC Ensembl
Outerchr9:66193452..66281950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3886474
hg1986474
hg1886499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4388e59
Supporting Variantsessv8697047
SamplesNA19240
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3451882
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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