A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891892



Internal ID19186288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122783827..122789343hg38UCSC Ensembl
Outerchr10:122783827..122789343hg38UCSC Ensembl
Innerchr10:124543343..124548859hg19UCSC Ensembl
Outerchr10:124543343..124548859hg19UCSC Ensembl
Innerchr10:124533333..124538849hg18UCSC Ensembl
Outerchr10:124533333..124538849hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385517
hg195517
hg185517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784273
Samples
Known GenesFLJ46361
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891892
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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