A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434043



Internal ID15280998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65259074..65280788hg38UCSC Ensembl
Innerchr9:65260078..65279788hg38UCSC Ensembl
Outerchr9:65258187..65281787hg38UCSC Ensembl
chr9:42721656..42743354hg19UCSC Ensembl
Innerchr9:42722656..42742354hg19UCSC Ensembl
Outerchr9:42720656..42744354hg19UCSC Ensembl
chr9:42711652..42733350hg18UCSC Ensembl
Innerchr9:42712652..42732350hg18UCSC Ensembl
Outerchr9:42710652..42734350hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3821715
hg1921699
hg1821699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337e59
Supporting Variantsessv8696747
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434043
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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