A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3349555



Internal ID15196537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133511509..133513007hg38UCSC Ensembl
Innerchr9:133512007..133512509hg38UCSC Ensembl
Outerchr9:133510509..133514007hg38UCSC Ensembl
chr9:136376631..136378129hg19UCSC Ensembl
Innerchr9:136377129..136377631hg19UCSC Ensembl
Outerchr9:136375631..136379129hg19UCSC Ensembl
chr9:135366452..135367950hg18UCSC Ensembl
Innerchr9:135367452..135366950hg18UCSC Ensembl
Outerchr9:135365452..135368950hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696541
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3349555
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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