A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893899



Internal ID18838067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25652944..25747681hg38UCSC Ensembl
Outerchr4:25652944..25747681hg38UCSC Ensembl
Innerchr4:25654566..25749303hg19UCSC Ensembl
Outerchr4:25654566..25749303hg19UCSC Ensembl
Innerchr4:25263664..25358401hg18UCSC Ensembl
Outerchr4:25263664..25358401hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3894738
hg1994738
hg1894738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781395
Samples
Known GenesSEL1L3, SLC34A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893899
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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