A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892320



Internal ID18836454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23486150..23650003hg38UCSC Ensembl
Outerchr13:23486150..23650003hg38UCSC Ensembl
Innerchr13:24060289..24224142hg19UCSC Ensembl
Outerchr13:24060289..24224142hg19UCSC Ensembl
Innerchr13:22958289..23122142hg18UCSC Ensembl
Outerchr13:22958289..23122142hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38163854
hg19163854
hg18163854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800294
Samples
Known GenesLINC00327, TNFRSF19
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892320
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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