A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892206



Internal ID19183026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:60725485..61308324hg38UCSC Ensembl
Outerchr12:60725485..61309626hg38UCSC Ensembl
Innerchr12:61119266..61702105hg19UCSC Ensembl
Outerchr12:61119266..61703407hg19UCSC Ensembl
Innerchr12:59405533..59988372hg18UCSC Ensembl
Outerchr12:59405533..59989674hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38584142
hg19584142
hg18584142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785585, essv25779900
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892206
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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