A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3439544



Internal ID15286497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76836361..76836370hg38UCSC Ensembl
Innerchr9:76836354..76836377hg38UCSC Ensembl
Outerchr9:76836345..76836386hg38UCSC Ensembl
chr9:79451277..79451286hg19UCSC Ensembl
Innerchr9:79451270..79451293hg19UCSC Ensembl
Outerchr9:79451261..79451302hg19UCSC Ensembl
chr9:78641097..78641106hg18UCSC Ensembl
Innerchr9:78641113..78641090hg18UCSC Ensembl
Outerchr9:78641081..78641122hg18UCSC Ensembl
Cytoband9q21.13
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 Variantsessv8677447, essv8677448, essv8677445, essv8677446
SamplesNA19238, NA12878, NA12892, NA19240
Known GenesPRUNE2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3439544
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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