A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3391242



Internal ID15238209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138261081..138262979hg38UCSC Ensembl
Innerchr9:138261979..138262081hg38UCSC Ensembl
Outerchr9:138260081..138262981hg38UCSC Ensembl
chr9:141151531..141153429hg19UCSC Ensembl
Innerchr9:141152429..141152531hg19UCSC Ensembl
Outerchr9:141150531..141153431hg19UCSC Ensembl
chr9:140271352..140273250hg18UCSC Ensembl
Innerchr9:140272352..140272250hg18UCSC Ensembl
Outerchr9:140270352..140273252hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4549e59
Supporting Variantsessv8696607
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3391242
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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