A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892404



Internal ID19183224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83528305..83583792hg38UCSC Ensembl
Outerchr13:83528305..83591492hg38UCSC Ensembl
Innerchr13:84102440..84157927hg19UCSC Ensembl
Outerchr13:84102440..84165627hg19UCSC Ensembl
Innerchr13:83000441..83055928hg18UCSC Ensembl
Outerchr13:83000441..83063628hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3863188
hg1963188
hg1863188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780631, essv25786494, essv25785887
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892404
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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