A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3448639



Internal ID15295588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62888408..62892906hg38UCSC Ensembl
Innerchr9:62889408..62891906hg38UCSC Ensembl
Outerchr9:62887408..62893906hg38UCSC Ensembl
chr9:66544232..66548730hg19UCSC Ensembl
Innerchr9:66545232..66547730hg19UCSC Ensembl
Outerchr9:66543232..66549730hg19UCSC Ensembl
chr9:66284052..66288550hg18UCSC Ensembl
Innerchr9:66285052..66287550hg18UCSC Ensembl
Outerchr9:66283052..66289550hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg384499
hg194499
hg184499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697056
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3448639
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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