A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890766



Internal ID19185068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:166855307..166883792hg38UCSC Ensembl
Outerchr5:166855307..166883792hg38UCSC Ensembl
Innerchr5:166282312..166310797hg19UCSC Ensembl
Outerchr5:166282312..166310797hg19UCSC Ensembl
Innerchr5:166214890..166243375hg18UCSC Ensembl
Outerchr5:166214890..166243375hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3828486
hg1928486
hg1828486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799631
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890766
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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