A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890702



Internal ID19185004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106470016..106574299hg38UCSC Ensembl
Outerchr5:106455568..106620643hg38UCSC Ensembl
Innerchr5:105805717..105910000hg19UCSC Ensembl
Outerchr5:105791269..105956344hg19UCSC Ensembl
Innerchr5:105833616..105937899hg18UCSC Ensembl
Outerchr5:105819168..105984243hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38165076
hg19165076
hg18165076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781444, essv25787649, essv25800576, essv25800006, essv25799650
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890702
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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