A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894174



Internal ID19185243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:34278321..34395767hg38UCSC Ensembl
Outerchr5:34278321..34395767hg38UCSC Ensembl
Innerchr5:34278426..34395872hg19UCSC Ensembl
Outerchr5:34278426..34395872hg19UCSC Ensembl
Innerchr5:34314183..34431629hg18UCSC Ensembl
Outerchr5:34314183..34431629hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38117447
hg19117447
hg18117447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791868
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894174
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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