A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697057



Internal ID13661775
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 Flag0
Merged StatusS
Merged Variantsesv3378699
Supporting Variants
SamplesNA12878
Known GenesMGC21881
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697057
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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