A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890680



Internal ID18838296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101142727..101508337hg38UCSC Ensembl
Outerchr5:101142727..101508337hg38UCSC Ensembl
Innerchr5:100478431..100844041hg19UCSC Ensembl
Outerchr5:100478431..100844041hg19UCSC Ensembl
Innerchr5:100506330..100871940hg18UCSC Ensembl
Outerchr5:100506330..100871940hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38365611
hg19365611
hg18365611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798516
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890680
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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