A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892438



Internal ID19183258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101566377..101647763hg38UCSC Ensembl
Outerchr13:101554523..101650500hg38UCSC Ensembl
Innerchr13:102218728..102300113hg19UCSC Ensembl
Outerchr13:102206874..102302850hg19UCSC Ensembl
Innerchr13:101016729..101098114hg18UCSC Ensembl
Outerchr13:101004875..101100851hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3895978
hg1995977
hg1895977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796555, essv25796359, essv25784122, essv25796833
Samples
Known GenesITGBL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892438
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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