A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3376056



Internal ID15223029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103992649..103992760hg38UCSC Ensembl
Innerchr10:103992656..103992751hg38UCSC Ensembl
Outerchr10:103992640..103992767hg38UCSC Ensembl
chr10:105752407..105752518hg19UCSC Ensembl
Innerchr10:105752414..105752509hg19UCSC Ensembl
Outerchr10:105752398..105752525hg19UCSC Ensembl
chr10:105742397..105742508hg18UCSC Ensembl
Innerchr10:105742404..105742499hg18UCSC Ensembl
Outerchr10:105742388..105742515hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38112
hg19112
hg18112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8670413, essv8670414, essv8670411, essv8670412, essv8670410
SamplesNA12891, NA19238, NA12878, NA12892, NA19240
Known GenesSLK
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3376056
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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