A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781395



Internal ID18835655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25652944..25747681hg38UCSC Ensembl
Innerchr4:25654566..25749303hg19UCSC Ensembl
Innerchr4:25263664..25358401hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3894738
hg1994738
hg1894738
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893899
Supporting Variants
Samples
Known GenesSEL1L3, SLC34A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781395
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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