A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3387957



Internal ID15234926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63139760..63144958hg38UCSC Ensembl
Innerchr9:63140760..63143958hg38UCSC Ensembl
Outerchr9:63138760..63145958hg38UCSC Ensembl
chr9:67044732..67049930hg19UCSC Ensembl
Innerchr9:67045732..67048930hg19UCSC Ensembl
Outerchr9:67043732..67050930hg19UCSC Ensembl
chr9:66784552..66789750hg18UCSC Ensembl
Innerchr9:66785552..66788750hg18UCSC Ensembl
Outerchr9:66783552..66790750hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385199
hg195199
hg185199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697101
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3387957
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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