A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302903



Internal ID15149851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118846453..118854358hg38UCSC Ensembl
Innerchr9:118846553..118854258hg38UCSC Ensembl
Outerchr9:118846353..118854458hg38UCSC Ensembl
chr9:121608731..121616636hg19UCSC Ensembl
Innerchr9:121608831..121616536hg19UCSC Ensembl
Outerchr9:121608631..121616736hg19UCSC Ensembl
chr9:120648552..120656457hg18UCSC Ensembl
Innerchr9:120648652..120656357hg18UCSC Ensembl
Outerchr9:120648452..120656557hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg387906
hg197906
hg187906
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7737240
SamplesNA18522
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302903
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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