A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697092



Internal ID15060766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63109760..63126558hg38UCSC Ensembl
Innerchr9:63110760..63125558hg38UCSC Ensembl
Outerchr9:63108760..63127558hg38UCSC Ensembl
chr9:67014732..67031530hg19UCSC Ensembl
Innerchr9:67015732..67030530hg19UCSC Ensembl
Outerchr9:67013732..67032530hg19UCSC Ensembl
chr9:66754552..66771350hg18UCSC Ensembl
Innerchr9:66755552..66770350hg18UCSC Ensembl
Outerchr9:66753552..66772350hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3816799
hg1916799
hg1816799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3448720
Supporting Variants
SamplesNA19239
Known GenesLOC286297
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697092
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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