A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797287



Internal ID19165818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44835599..44849479hg38UCSC Ensembl
Innerchr13:45409735..45423615hg19UCSC Ensembl
Innerchr13:44307735..44321615hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3813881
hg1913881
hg1813881
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892339
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797287
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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