A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892336



Internal ID18836470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43420155..43603151hg38UCSC Ensembl
Outerchr13:43420155..43603319hg38UCSC Ensembl
Innerchr13:43994291..44177287hg19UCSC Ensembl
Outerchr13:43994291..44177455hg19UCSC Ensembl
Innerchr13:42892291..43075287hg18UCSC Ensembl
Outerchr13:42892291..43075455hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38183165
hg19183165
hg18183165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778413, essv25780775
Samples
Known GenesENOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892336
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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