A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784590



Internal ID19177063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168634072..168719722hg38UCSC Ensembl
Innerchr3:168351860..168437510hg19UCSC Ensembl
Innerchr3:169834554..169920204hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3885651
hg1985651
hg1885651
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893813
Supporting Variants
Samples
Known GenesEGFEM1P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784590
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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