A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3339609



Internal ID15186596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1850722..1850733hg38UCSC Ensembl
Innerchr9:1850717..1850738hg38UCSC Ensembl
Outerchr9:1850706..1850749hg38UCSC Ensembl
chr9:1850722..1850733hg19UCSC Ensembl
Innerchr9:1850717..1850738hg19UCSC Ensembl
Outerchr9:1850706..1850749hg19UCSC Ensembl
chr9:1840722..1840733hg18UCSC Ensembl
Innerchr9:1840738..1840717hg18UCSC Ensembl
Outerchr9:1840706..1840749hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38276
hg19276
hg18276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8943356, essv8943351, essv8943355, essv8943352, essv8943344, essv8943345, essv8943346, essv8943340, essv8943353, essv8943342, essv8943343, essv8943341, essv8943350, essv8943349, essv8943354, essv8943347
SamplesNA18502, NA18861, NA18508, NA18504, NA19190, NA18870, NA18489, NA19138, NA19137, NA19172, NA18516, NA19114, NA19099, NA19257, NA19225, NA18501
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3339609
Frequency
Sample Size185
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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