A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791284



Internal ID19180876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:181738105..182088461hg38UCSC Ensembl
Innerchr4:182659258..183009614hg19UCSC Ensembl
Innerchr4:182896252..183246608hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38350357
hg19350357
hg18350357
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894087
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=111
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791284
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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