A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799150



Internal ID19160159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:124749182..124778759hg38UCSC Ensembl
Innerchr4:125670337..125699914hg19UCSC Ensembl
Innerchr4:125889787..125919364hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3829578
hg1929578
hg1829578
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894024
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799150
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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