A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784273



Internal ID19171586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122783827..122789343hg38UCSC Ensembl
Innerchr10:124543343..124548859hg19UCSC Ensembl
Innerchr10:124533333..124538849hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385517
hg195517
hg185517
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891892
Supporting Variants
Samples
Known GenesFLJ46361
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784273
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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