A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779890



Internal ID19160674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54332575..54884124hg38UCSC Ensembl
Innerchr13:54906710..55458259hg19UCSC Ensembl
Innerchr13:53804711..54356260hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38551550
hg19551550
hg18551550
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892346
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=113
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779890
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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