A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3383589



Internal ID15230559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70358691..70358755hg38UCSC Ensembl
Innerchr9:70358684..70358760hg38UCSC Ensembl
Outerchr9:70358622..70358824hg38UCSC Ensembl
chr9:72973607..72973671hg19UCSC Ensembl
Innerchr9:72973600..72973676hg19UCSC Ensembl
Outerchr9:72973538..72973740hg19UCSC Ensembl
chr9:72163427..72163491hg18UCSC Ensembl
Innerchr9:72163496..72163420hg18UCSC Ensembl
Outerchr9:72163358..72163560hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38288
hg19288
hg18288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8677422
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3383589
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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