A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890724



Internal ID18838340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:117373037..117384655hg38UCSC Ensembl
Outerchr5:117373037..117384655hg38UCSC Ensembl
Innerchr5:116708733..116720351hg19UCSC Ensembl
Outerchr5:116708733..116720351hg19UCSC Ensembl
Innerchr5:116736632..116748250hg18UCSC Ensembl
Outerchr5:116736632..116748250hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3811619
hg1911619
hg1811619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787574
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890724
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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