A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785250



Internal ID19176377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:110063399..110076619hg38UCSC Ensembl
Innerchr4:110984555..110997775hg19UCSC Ensembl
Innerchr4:111204004..111217224hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3813221
hg1913221
hg1813221
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894004
Supporting Variants
Samples
Known GenesELOVL6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785250
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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