A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3384120



Internal ID15231090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133769437..133772135hg38UCSC Ensembl
Innerchr10:133770437..133771135hg38UCSC Ensembl
Outerchr10:133768437..133773135hg38UCSC Ensembl
chr10:135506762..135509460hg19UCSC Ensembl
Innerchr10:135507762..135508460hg19UCSC Ensembl
Outerchr10:135505762..135510460hg19UCSC Ensembl
chr10:135356752..135359450hg18UCSC Ensembl
Innerchr10:135357752..135358450hg18UCSC Ensembl
Outerchr10:135355752..135360450hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8687987
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3384120
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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