A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800294



Internal ID18826087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23486150..23650003hg38UCSC Ensembl
Innerchr13:24060289..24224142hg19UCSC Ensembl
Innerchr13:22958289..23122142hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38163854
hg19163854
hg18163854
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892320
Supporting Variants
Samples
Known GenesLINC00327, TNFRSF19
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=45
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800294
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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