A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892421



Internal ID19183241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90350411..90432319hg38UCSC Ensembl
Outerchr13:90350411..90432319hg38UCSC Ensembl
Innerchr13:91002665..91084573hg19UCSC Ensembl
Outerchr13:91002665..91084573hg19UCSC Ensembl
Innerchr13:89800666..89882574hg18UCSC Ensembl
Outerchr13:89800666..89882574hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3881909
hg1981909
hg1881909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779768
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892421
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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