A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7735080



Internal ID14129194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125824874..125825093hg38UCSC Ensembl
Outerchr10:125824674..125825293hg38UCSC Ensembl
Innerchr10:127513443..127513662hg19UCSC Ensembl
Outerchr10:127513243..127513862hg19UCSC Ensembl
Innerchr10:127503433..127503652hg18UCSC Ensembl
Outerchr10:127503233..127503852hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38620
hg19620
hg18620
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302844
Supporting Variants
SamplesNA18566
Known GenesBCCIP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7735080
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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