A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788578



Internal ID19182940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:117394404..117421060hg38UCSC Ensembl
Innerchr4:118315560..118342216hg19UCSC Ensembl
Innerchr4:118535008..118561664hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3826657
hg1926657
hg1826657
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894013
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788578
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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