A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894102



Internal ID19184956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189904623..190005977hg38UCSC Ensembl
Outerchr4:189880922..190044201hg38UCSC Ensembl
Innerchr4:190825778..190927132hg19UCSC Ensembl
Outerchr4:190802077..190965356hg19UCSC Ensembl
Innerchr4:191062772..191164126hg18UCSC Ensembl
Outerchr4:191039071..191202350hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38163280
hg19163280
hg18163280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790674, essv25791920
Samples
Known GenesFRG1, FRG2, LOC100288255, LOC283788
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894102
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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