A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893788



Internal ID19184608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153527923..153579259hg38UCSC Ensembl
Outerchr3:153527923..153579259hg38UCSC Ensembl
Innerchr3:153245712..153297048hg19UCSC Ensembl
Outerchr3:153245712..153297048hg19UCSC Ensembl
Innerchr3:154728402..154779738hg18UCSC Ensembl
Outerchr3:154728402..154779738hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3851337
hg1951337
hg1851337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789566
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893788
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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