A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790674



Internal ID19162719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189904623..190005977hg38UCSC Ensembl
Innerchr4:190825778..190927132hg19UCSC Ensembl
Innerchr4:191062772..191164126hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38101355
hg19101355
hg18101355
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894102
Supporting Variants
Samples
Known GenesFRG1, LOC283788
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790674
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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