A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677422



Internal ID15057595
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 StatusS
Merged Variantsesv3383589
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677422
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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