A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3402119



Internal ID15249081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138261081..138262879hg38UCSC Ensembl
Innerchr9:138261879..138262081hg38UCSC Ensembl
Outerchr9:138260081..138262981hg38UCSC Ensembl
chr9:141151531..141153329hg19UCSC Ensembl
Innerchr9:141152329..141152531hg19UCSC Ensembl
Outerchr9:141150531..141153431hg19UCSC Ensembl
chr9:140271352..140273150hg18UCSC Ensembl
Innerchr9:140272352..140272150hg18UCSC Ensembl
Outerchr9:140270352..140273252hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4549e59
Supporting Variantsessv8696605
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3402119
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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