A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892406



Internal ID19183226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83960759..84050777hg38UCSC Ensembl
Outerchr13:83960759..84062535hg38UCSC Ensembl
Innerchr13:84534894..84624912hg19UCSC Ensembl
Outerchr13:84534894..84636670hg19UCSC Ensembl
Innerchr13:83432895..83522913hg18UCSC Ensembl
Outerchr13:83432895..83534671hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38101777
hg19101777
hg18101777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798171, essv25801064
Samples
Known GenesMIR548F1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892406
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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