A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894203



Internal ID19185272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64436478..64473681hg38UCSC Ensembl
Outerchr5:64414728..64476234hg38UCSC Ensembl
Innerchr5:63732305..63769508hg19UCSC Ensembl
Outerchr5:63710555..63772061hg19UCSC Ensembl
Innerchr5:63768061..63805264hg18UCSC Ensembl
Outerchr5:63746311..63807817hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3861507
hg1961507
hg1861507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797799, essv25783728, essv25785875, essv25781922, essv25796710, essv25782170, essv25782799, essv25800478, essv25797873, essv25782855, essv25786634, essv25785478, essv25783919
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894203
Frequency
Sample Size3017
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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