A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8670414



Internal ID13703998
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 StatusS
Merged Variantsesv3376056
Supporting Variants
SamplesNA12891
Known GenesSLK
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8670414
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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