A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892346



Internal ID19183166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54332575..54855829hg38UCSC Ensembl
Outerchr13:54332575..54884124hg38UCSC Ensembl
Innerchr13:54906710..55429964hg19UCSC Ensembl
Outerchr13:54906710..55458259hg19UCSC Ensembl
Innerchr13:53804711..54327965hg18UCSC Ensembl
Outerchr13:53804711..54356260hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38551550
hg19551550
hg18551550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779946, essv25779890
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892346
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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