A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784204



Internal ID19161759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11438322..11458256hg38UCSC Ensembl
Innerchr4:11439946..11459880hg19UCSC Ensembl
Innerchr4:11049044..11068978hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3819935
hg1919935
hg1819935
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893881
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784204
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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