A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892327



Internal ID18836461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34080781..34227911hg38UCSC Ensembl
Outerchr13:34080781..34227911hg38UCSC Ensembl
Innerchr13:34654918..34802048hg19UCSC Ensembl
Outerchr13:34654918..34802048hg19UCSC Ensembl
Innerchr13:33552918..33700048hg18UCSC Ensembl
Outerchr13:33552918..33700048hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38147131
hg19147131
hg18147131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778967, essv25783227
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892327
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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