A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892395



Internal ID19183215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:78077164..78100255hg38UCSC Ensembl
Outerchr13:78077164..78100255hg38UCSC Ensembl
Innerchr13:78651299..78674390hg19UCSC Ensembl
Outerchr13:78651299..78674390hg19UCSC Ensembl
Innerchr13:77549300..77572391hg18UCSC Ensembl
Outerchr13:77549300..77572391hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3823092
hg1923092
hg1823092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785853
Samples
Known GenesRNF219-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892395
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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