A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892339



Internal ID19183159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44841057..44849479hg38UCSC Ensembl
Outerchr13:44835599..44855298hg38UCSC Ensembl
Innerchr13:45415193..45423615hg19UCSC Ensembl
Outerchr13:45409735..45429434hg19UCSC Ensembl
Innerchr13:44313193..44321615hg18UCSC Ensembl
Outerchr13:44307735..44327434hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3819700
hg1919700
hg1819700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797287, essv25781248
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892339
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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