A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892397



Internal ID19183217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81148093..81187865hg38UCSC Ensembl
Outerchr13:81138737..81188766hg38UCSC Ensembl
Innerchr13:81722228..81762000hg19UCSC Ensembl
Outerchr13:81712872..81762901hg19UCSC Ensembl
Innerchr13:80620229..80660001hg18UCSC Ensembl
Outerchr13:80610873..80660902hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3850030
hg1950030
hg1850030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796145, essv25796350, essv25781390
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892397
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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