A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894168



Internal ID19185237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29721349..29768235hg38UCSC Ensembl
Outerchr5:29721349..29768235hg38UCSC Ensembl
Innerchr5:29721456..29768342hg19UCSC Ensembl
Outerchr5:29721456..29768342hg19UCSC Ensembl
Innerchr5:29757213..29804099hg18UCSC Ensembl
Outerchr5:29757213..29804099hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3846887
hg1946887
hg1846887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788951
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894168
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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