A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302874



Internal ID14803136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86524717..86524819hg38UCSC Ensembl
Innerchr10:86524768..86524768hg38UCSC Ensembl
Outerchr10:86524617..86524919hg38UCSC Ensembl
chr10:88284474..88284576hg19UCSC Ensembl
Innerchr10:88284525..88284525hg19UCSC Ensembl
Outerchr10:88284374..88284676hg19UCSC Ensembl
chr10:88274454..88274556hg18UCSC Ensembl
Innerchr10:88274505..88274505hg18UCSC Ensembl
Outerchr10:88274354..88274656hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38103
hg19103
hg18103
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv469e59
Supporting Variantsessv7738074, essv7737314, essv7732560, essv7732473, essv7732024, essv7735331, essv7734989, essv7735178, essv7733746, essv7738549, essv7732368, essv7736257, essv7734223, essv7733494, essv7736974, essv7734842, essv7731873, essv7732762, essv7734509, essv7736937, essv7735489, essv7734036, essv7739243, essv7738216, essv7733861, essv7733079, essv7737270, essv7734161, essv7736134, essv7737080, essv7737463, essv7739169, essv7733358, essv7737150
SamplesNA18502, NA18947, NA18861, NA18508, NA10851, NA12414, NA18507, NA11920, NA11931, NA18870, NA18550, NA12891, NA18916, NA12287, NA19138, NA19137, NA19238, NA12878, NA11894, NA12892, NA19225, NA18858, NA18945, NA19108, NA18517, NA19240, NA07037, NA18501, NA19093, NA18505, NA12006, NA18511, NA12776, NA18965
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302874
Frequency
Sample Size185
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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