A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780232



Internal ID18818370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4196512..4421324hg38UCSC Ensembl
Innerchr3:4238196..4463008hg19UCSC Ensembl
Innerchr3:4213196..4438008hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38224813
hg19224813
hg18224813
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893640
Supporting Variants
Samples
Known GenesSETMAR, SUMF1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=79
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780232
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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