A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3378699



Internal ID15225672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62898408..62933106hg38UCSC Ensembl
Innerchr9:62899408..62932106hg38UCSC Ensembl
Outerchr9:62897408..62934106hg38UCSC Ensembl
chr9:66554232..66588930hg19UCSC Ensembl
Innerchr9:66555232..66587930hg19UCSC Ensembl
Outerchr9:66553232..66589930hg19UCSC Ensembl
chr9:66294052..66328750hg18UCSC Ensembl
Innerchr9:66295052..66327750hg18UCSC Ensembl
Outerchr9:66293052..66329750hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3834699
hg1934699
hg1834699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697057
SamplesNA12878
Known GenesMGC21881
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3378699
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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