A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892286



Internal ID18836420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132381904..132460553hg38UCSC Ensembl
Outerchr12:132381904..132474050hg38UCSC Ensembl
Innerchr12:132958490..133037139hg19UCSC Ensembl
Outerchr12:132958490..133050636hg19UCSC Ensembl
Innerchr12:131468563..131547212hg18UCSC Ensembl
Outerchr12:131468563..131560709hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3892147
hg1992147
hg1892147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782728, essv25780119, essv25784026
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892286
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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