A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894166



Internal ID19185235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29497767..29574668hg38UCSC Ensembl
Outerchr5:29497767..29574668hg38UCSC Ensembl
Innerchr5:29497874..29574775hg19UCSC Ensembl
Outerchr5:29497874..29574775hg19UCSC Ensembl
Innerchr5:29533631..29610532hg18UCSC Ensembl
Outerchr5:29533631..29610532hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3876902
hg1976902
hg1876902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789716
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894166
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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