A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892313



Internal ID19183133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22299346..22750123hg38UCSC Ensembl
Outerchr13:22299346..22750123hg38UCSC Ensembl
Innerchr13:22873485..23324262hg19UCSC Ensembl
Outerchr13:22873485..23324262hg19UCSC Ensembl
Innerchr13:21771485..22222262hg18UCSC Ensembl
Outerchr13:21771485..22222262hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38450778
hg19450778
hg18450778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787703
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892313
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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