A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789566



Internal ID19165525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153527923..153579259hg38UCSC Ensembl
Innerchr3:153245712..153297048hg19UCSC Ensembl
Innerchr3:154728402..154779738hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3851337
hg1951337
hg1851337
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893788
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789566
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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