A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893640



Internal ID18837774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4196512..4421324hg38UCSC Ensembl
Outerchr3:4196512..4421324hg38UCSC Ensembl
Innerchr3:4238196..4463008hg19UCSC Ensembl
Outerchr3:4238196..4463008hg19UCSC Ensembl
Innerchr3:4213196..4438008hg18UCSC Ensembl
Outerchr3:4213196..4438008hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38224813
hg19224813
hg18224813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780232
Samples
Known GenesSETMAR, SUMF1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893640
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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