A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3365978



Internal ID15212955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80655316..80656914hg38UCSC Ensembl
Innerchr10:80655914..80656316hg38UCSC Ensembl
Outerchr10:80654316..80657914hg38UCSC Ensembl
chr10:82415072..82416670hg19UCSC Ensembl
Innerchr10:82415670..82416072hg19UCSC Ensembl
Outerchr10:82414072..82417670hg19UCSC Ensembl
chr10:82405052..82406650hg18UCSC Ensembl
Innerchr10:82406052..82405650hg18UCSC Ensembl
Outerchr10:82404052..82407650hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688143
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3365978
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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