A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894199



Internal ID19185268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:62688021..62844210hg38UCSC Ensembl
Outerchr5:62683162..62844210hg38UCSC Ensembl
Innerchr5:61983848..62140037hg19UCSC Ensembl
Outerchr5:61978989..62140037hg19UCSC Ensembl
Innerchr5:62019604..62175793hg18UCSC Ensembl
Outerchr5:62014745..62175793hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38161049
hg19161049
hg18161049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791833, essv25788484, essv25789303, essv25792212
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894199
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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